Publications by authors named "Hyung-Goo Kim"

62Publications

Long-Term Follow-Up and Treatment of a Female With Complete Estrogen Insensitivity.

J Clin Endocrinol Metab 2020 May;105(5)

Medical College of Georgia at Augusta University, Section of Reproductive Endocrinology, Infertility, & Genetics, Augusta, Georgia.

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http://dx.doi.org/10.1210/clinem/dgaa106DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7108680PMC
May 2020

The Use of Whole Exome Sequencing in a Cohort of Transgender Individuals to Identify Rare Genetic Variants.

Sci Rep 2019 12 27;9(1):20099. Epub 2019 Dec 27.

Section of Reproductive Endocrinology, Infertility, & Genetics, Department of Obstetrics & Gynecology, Medical College of Georgia, Augusta University, Augusta, Georgia, United States.

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http://dx.doi.org/10.1038/s41598-019-53500-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934803PMC
December 2019

The Body Size of Stimulus Conspecifics Affects Social Preference in a Binary Choice Task in Wild-Type, But Not in Mutant, Zebrafish.

Zebrafish 2019 06 6;16(3):262-267. Epub 2019 May 6.

1 Department of Biology, Chungnam National University, Daejeon, South Korea.

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http://dx.doi.org/10.1089/zeb.2018.1717DOI Listing
June 2019

Development of novel biocompatible thermosensitive anti-adhesive agents using human-derived acellular dermal matrix.

PLoS One 2019 22;14(2):e0212583. Epub 2019 Feb 22.

Department of Dermatology and Cutaneous Biology Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0212583PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6386309PMC
November 2019

Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia.

Mol Cytogenet 2018 3;11:13. Epub 2018 Feb 3.

7Section of Reproductive Endocrinology, Infertility, & Genetics, Department of Obstetrics & Gynecology Medical College of Georgia at Augusta University, Augusta, GA USA.

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http://dx.doi.org/10.1186/s13039-018-0359-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797403PMC
February 2018

Chd7 Is Critical for Early T-Cell Development and Thymus Organogenesis in Zebrafish.

Am J Pathol 2018 04 31;188(4):1043-1058. Epub 2018 Jan 31.

Institute of Life Science, Nanchang University, Nanchang, China; School of Life Sciences, Nanchang University, Nanchang, China; Jiangxi Provincial Collaborative Innovation Center for Cardiovascular, Digestive and Neuropsychiatric Diseases, Nanchang, China. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00029440173066
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http://dx.doi.org/10.1016/j.ajpath.2017.12.005DOI Listing
April 2018

Genetic analysis of Mayer-Rokitansky-Kuster-Hauser syndrome in a large cohort of families.

Fertil Steril 2017 07 7;108(1):145-151.e2. Epub 2017 Jun 7.

Section of Reproductive Endocrinology, Infertility, and Genetics, Department of Obstetrics and Gynecology, Medical College of Georgia, Augusta University, Augusta, Georgia; Department of Neuroscience and Regenerative Medicine, Medical College of Georgia, Augusta University, Augusta, Georgia; Department of Physiology, Medical College of Georgia, Augusta University, Augusta, Georgia. Electronic address:

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http://dx.doi.org/10.1016/j.fertnstert.2017.05.017DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5770980PMC
July 2017

Transcriptome Analysis Revealed Impaired cAMP Responsiveness in PHF21A-Deficient Human Cells.

Neuroscience 2018 02 29;370:170-180. Epub 2017 May 29.

Department of Human Genetics, University of Michigan, Ann Arbor, MI, USA. Electronic address:

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http://dx.doi.org/10.1016/j.neuroscience.2017.05.031DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5708152PMC
February 2018

Steric Clash in the SET Domain of Histone Methyltransferase NSD1 as a Cause of Sotos Syndrome and Its Genetic Heterogeneity in a Brazilian Cohort.

Genes (Basel) 2016 Nov 9;7(11). Epub 2016 Nov 9.

Section of Reproductive Endocrinology, Infertility & Genetics, Department of Obstetrics and Gynecology, Department of Neuroscience and Regenerative Medicine, Medical College of Georgia, Augusta University, 1120 15th Street, Augusta, GA 30912, USA.

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http://dx.doi.org/10.3390/genes7110096DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5126782PMC
November 2016

The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability.

Mol Cytogenet 2016 29;9:74. Epub 2016 Sep 29.

Section of Reproductive Endocrinology, Infertility & Genetics, Department of Obstetrics & Gynecology, Augusta University, Augusta, GA 30912 USA ; Department of Neuroscience and Regenerative Medicine, Augusta University, 1120 15th Street, Augusta, GA 30912 USA.

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http://dx.doi.org/10.1186/s13039-016-0286-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5041540PMC
September 2016

A microdeletion at Xq22.2 implicates a glycine receptor GLRA4 involved in intellectual disability, behavioral problems and craniofacial anomalies.

BMC Neurol 2016 Aug 9;16:132. Epub 2016 Aug 9.

Department of Obstetrics & Gynecology, Section of Reproductive Endocrinology, Infertility & Genetics, Medical College of Georgia, Augusta University, 1120 15th Street, Augusta, GA, 30912, USA.

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http://dx.doi.org/10.1186/s12883-016-0642-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979147PMC
August 2016

Targeted next generation sequencing approach identifies eighteen new candidate genes in normosmic hypogonadotropic hypogonadism and Kallmann syndrome.

Mol Cell Endocrinol 2016 12 5;437:86-96. Epub 2016 Aug 5.

Section of Reproductive Endocrinology, Infertility, & Genetics, Department of Obstetrics & Gynecology, Medical College of Georgia, Augusta University, Augusta, GA, United States; Department of Neuroscience and Regenerative Medicine, Medical College of Georgia, Augusta University, Augusta, GA, United States; Department of Physiology, Medical College of Georgia, Augusta University, Augusta, GA, United States. Electronic address:

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http://dx.doi.org/10.1016/j.mce.2016.08.007DOI Listing
December 2016

A balanced chromosomal translocation involving chromosomes 3 and 16 in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome reveals new candidate genes at 3p22.3 and 16p13.3.

Mol Cytogenet 2016 30;9:57. Epub 2016 Jul 30.

Section of Reproductive Endocrinology, Infertility, & Genetics, Department of Obstetrics & Gynecology, Medical College of Georgia, Augusta University, Augusta, GA USA ; Department of Neuroscience & Regenerative Medicine, Augusta University, Augusta, GA 30912 USA ; Department of Physiology, Medical College of Georgia, Augusta University, Augusta, GA 30912 USA.

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http://dx.doi.org/10.1186/s13039-016-0264-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967518PMC
August 2016

An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability.

Hum Genet 2016 07 22;135(7):757-71. Epub 2016 Apr 22.

Section of Reproductive Endocrinology, Infertility and Genetics, Department of Obstetrics and Gynecology, Augusta University, Augusta, GA, 30912, USA.

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http://dx.doi.org/10.1007/s00439-016-1668-4DOI Listing
July 2016

Comparative deletion mapping at 1p31.3-p32.2 implies NFIA responsible for intellectual disability coupled with macrocephaly and the presence of several other genes for syndromic intellectual disability.

Mol Cytogenet 2016 17;9:24. Epub 2016 Mar 17.

Department of Obstetrics & Gynecology, Augusta University, 1120 15th Street, Augusta, GA 30912 USA ; Department of Neuroscience and Regenerative Medicine, Medical College of Georgia, Augusta University, 1120 15th Street, Augusta, GA 30912 USA.

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http://dx.doi.org/10.1186/s13039-016-0234-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4797196PMC
March 2016

A microdeletion encompassing PHF21A in an individual with global developmental delay and craniofacial anomalies.

Am J Med Genet A 2015 Dec 3;167A(12):3011-8. Epub 2015 Sep 3.

Section of Reproductive Endocrinology, Infertility and Genetics, Department of Obstetrics and Gynecology, Georgia Regents University, Augusta, Georgia.

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http://dx.doi.org/10.1002/ajmg.a.37344DOI Listing
December 2015

Concomitant partial exon skipping by a unique missense mutation of RPS6KA3 causes Coffin-Lowry syndrome.

Gene 2016 Jan 20;575(1):42-7. Epub 2015 Aug 20.

Section of Reproductive Endocrinology, Infertility & Genetics, Department of Obstetrics & Gynecology, Georgia Regents University, Augusta, GA 30912, USA; Department of Neuroscience and Regenerative Medicine, Georgia Regents University, Augusta, GA 30912, USA. Electronic address:

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http://dx.doi.org/10.1016/j.gene.2015.08.032DOI Listing
January 2016

Expanding the Spectrum of Founder Mutations Causing Isolated Gonadotropin-Releasing Hormone Deficiency.

J Clin Endocrinol Metab 2015 Oct 24;100(10):E1378-85. Epub 2015 Jul 24.

Harvard Reproductive Endocrine Sciences Center and Reproductive Endocrine Unit (J.-H.C., R.B., N.D.S., J.E.H., L.P., C.L.B., W.F.C.), and Department of Medicine, Psychiatric, and Neurodevelopmental Genetics Unit (P.H.L.), Analytic and Translational Genetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, and Center for Human Genetic Research (J.F.G.), Massachusetts General Hospital, and Department of Genetics, Harvard Medical School, Boston, Massachusetts Boston, Massachusetts 02114; Department of Genetics (M.-L.K.), University Hospital, Caen, 14003, Caen Cedex, France; Department of Biology and Pathology of Human Reproduction in Bialystok (K.J.), Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Olsztyn, and Department of Reproduction and Gynecological Endocrinology (S.W.), Medical University of Bialystok, Sklodowskiej 24A, 15-276 Bialystok, Poland; Institute for Genetic Medicine (R.Q.), Newcastle University, Newcastle-upon-Tyne, NE1 3BZ, United Kingdom; Disciplina de Endocrinologia (A.C.L.), Hospital das Clinicas da Faculdade de Medicina, Universidade de Sao Paulo, 05403-900 Sao Paulo, Brazil; Laboratoire de Biochimie et Génétique Moléculaire (C.D.), Hôpital Cochin, Assistance Publique-Hôpitaux de Paris, Université Paris-Descartes, 75014 Paris, France; Departments of Molecular Endocrinology and Pediatrics (T.O.), Hamamatsu University of School of Medicine, Hamamatsu 431-3192, Japan; Section of Reproductive Endocrinology, Infertility, and Genetics (H.-G.K., L.C.L.), Departments of Obstetrics and Gynecology and Neuroscience and Regenerative Medicine, Medical College of Georgia at Georgia Regents University, Augusta, Georgia 30912; and Department of Pediatrics (J.-H.C.), Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul 138-736, Republic of Korea.

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http://dx.doi.org/10.1210/jc.2015-2262DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596034PMC
October 2015

Autism and Intellectual Disability-Associated KIRREL3 Interacts with Neuronal Proteins MAP1B and MYO16 with Potential Roles in Neurodevelopment.

PLoS One 2015 22;10(4):e0123106. Epub 2015 Apr 22.

J.C. Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, South Carolina, United States of America; Department of Genetics and Biochemistry, Clemson University, Clemson, South Carolina, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0123106PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4406691PMC
April 2016

Long-term follow-up of females with unbalanced X;Y translocations-reproductive and nonreproductive consequences.

Mol Cytogenet 2015 22;8:13. Epub 2015 Feb 22.

Department of Obstetrics & Gynecology, Medical College of Georgia, Georgia Regents University, Augusta, GA USA ; Section of Reproductive Endocrinology, Infertility, & Genetics, Medical College of Georgia, Georgia Regents University, Augusta, GA USA ; Section of Reproductive Endocrinology, Infertility, & Genetics, Department of Obstetrics & Gynecology, Medical College of Georgia, Georgia Regents University, 1120 15th Street, Augusta, GA USA.

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http://dx.doi.org/10.1186/s13039-015-0112-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4347569PMC
March 2015

NELF knockout is associated with impaired pubertal development and subfertility.

Mol Cell Endocrinol 2015 May 27;407:26-36. Epub 2015 Feb 27.

Section of Reproductive Endocrinology, Infertility, & Genetics, Department of Obstetrics & Gynecology; Department of Physiology; Georgia Regents University, Augusta, GA 30912, USA; Department of Neuroscience and Regenerative Medicine, Georgia Regents University, Augusta, GA 30912, USA; Department of Physiology, Georgia Regents University, Augusta, GA 30912, USA. Electronic address:

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http://dx.doi.org/10.1016/j.mce.2015.02.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4429764PMC
May 2015

Characterization and tissue incorporation of cross-linked human acellular dermal matrix.

Biomaterials 2015 Mar 14;44:195-205. Epub 2015 Jan 14.

Department of Plastic and Reconstructive Surgery, Institute for Human Tissue Restoration, Yonsei University College of Medicine, 50 Yonsei-ro, Seodaemun-gu, Seoul, Republic of Korea. Electronic address:

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http://dx.doi.org/10.1016/j.biomaterials.2014.12.004DOI Listing
March 2015

Interstitial microduplication at 2p11.2 in a patient with syndromic intellectual disability: 30-year follow-up.

Mol Cytogenet 2014 19;7:52. Epub 2014 Aug 19.

Section of Reproductive Endocrinology, Infertility & Genetics, Department of Obstetrics and Gynecology, Institute of Molecular Medicine and Genetics, Medical College of Georgia, Georgia Regents University, 1120 15th Street, Augusta, Georgia.

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http://dx.doi.org/10.1186/1755-8166-7-52DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4188067PMC
October 2014

The historical Coffin-Lowry syndrome family revisited: identification of two novel mutations of RPS6KA3 in three male patients.

Am J Med Genet A 2014 Sep 7;164A(9):2172-9. Epub 2014 Jul 7.

Section of Reproductive Endocrinology, Infertility & Genetics, Department of Obstetrics and Gynecology, Institute of Molecular Medicine and Genetics, Medical College of Georgia, Georgia Regents University, Augusta, Georgia.

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http://dx.doi.org/10.1002/ajmg.a.36488DOI Listing
September 2014

Epigenetic remodelling and dysregulation of DLGAP4 is linked with early-onset cerebellar ataxia.

Hum Mol Genet 2014 Dec 1;23(23):6163-76. Epub 2014 Jul 1.

Wilhelm Johannsen Centre for Functional Genome Research, Department of Cellular and Molecular Medicine, Faculty of Health Sciences, University of Copenhagen, Copenhagen N DK-2200, Denmark,

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http://dx.doi.org/10.1093/hmg/ddu337DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222360PMC
December 2014

Familial 46,XY sex reversal without campomelic dysplasia caused by a deletion upstream of the SOX9 gene.

Mol Cell Endocrinol 2014 Aug 4;393(1-2):1-7. Epub 2014 Jun 4.

Division of Reproductive Endocrinology and Infertility, Department of OB/GYN, University of Texas Southwestern Medical Center, Dallas, TX 75235, United States.

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http://dx.doi.org/10.1016/j.mce.2014.05.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4332518PMC
August 2014

Spectrum of genes involved in a unique case of Potocki Schaffer syndrome with a large chromosome 11 deletion.

Clin Neuropathol 2014 May-Jun;33(3):238-44

Institute of Pathology, Neuropathology Section, Jena University Hospital, Friedrich-Schiller-University, Jena, Institute of Neuropathology, Saarland University, School of Medicine, Homburg/S., Germany, Genetic Diagnostic Laboratory, Department of Laboratory Medicine, Children's Hospital Boston, Waltham, MA, Department of Obstetrics and Gynecology, Institute of Molecular Medicine and Genetics, Georgia Regents University, Augusta, GA, and Departments of Obstetrics, Gynecology, and Reproductive Biology and of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199189PMC
http://dx.doi.org/10.5414/np300691DOI Listing
July 2014

Differential expression of nasal embryonic LHRH factor (NELF) variants in immortalized GnRH neuronal cell lines.

Mol Cell Endocrinol 2014 Mar 4;383(1-2):32-7. Epub 2013 Dec 4.

Section of Reproductive Endocrinology, Infertility, & Genetics, Department of Obstetrics & Gynecology; Institute of Molecular Medicine and Genetics; Georgia Regents University, Augusta, GA 30912, USA. Electronic address:

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http://dx.doi.org/10.1016/j.mce.2013.11.020DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3930684PMC
March 2014

Delayed puberty and estrogen resistance in a woman with estrogen receptor α variant.

N Engl J Med 2013 Jul;369(2):164-71

Section of Reproductive Endocrinology, Infertility, and Genetics, Department of Obstetrics and Gynecology, Institute of Molecular Medicine and Genetics, and the Neuroscience Program, Medical College of Georgia, Georgia Regents University, Augusta, GA 30912, USA.

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http://dx.doi.org/10.1056/NEJMoa1303611DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3823379PMC
July 2013

Identification of HESX1 mutations in Kallmann syndrome.

Fertil Steril 2013 Jun 1;99(7):1831-7. Epub 2013 Mar 1.

Department of Obstetrics and Gynecology, Section of Reproductive Endocrinology, Infertility, and Genetics, Medical College of Georgia, Georgia Health Sciences University, Augusta, Georgia 30912, USA.

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http://dx.doi.org/10.1016/j.fertnstert.2013.01.149DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3888813PMC
June 2013

Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders.

Hum Mol Genet 2013 May 31;22(9):1816-25. Epub 2013 Jan 31.

School of Paediatrics and Reproductive Health, University of Adelaide, Adelaide, SA 5006, Australia.

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http://dx.doi.org/10.1093/hmg/ddt035DOI Listing
May 2013

The molecular basis of impaired follicle-stimulating hormone action: evidence from human mutations and mouse models.

Reprod Sci 2013 Mar 26;20(3):211-33. Epub 2012 Nov 26.

Department of Obstetrics & Gynecology, Section of Reproductive Endocrinology, Infertility, & Genetics, Medical College of Georgia, Georgia Health Sciences University Augusta, GA 30912, USA.

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http://dx.doi.org/10.1177/1933719112461184DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3823505PMC
March 2013

The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome.

Fertil Steril 2011 Dec 28;96(6):1424-1430.e6. Epub 2011 Oct 28.

Section of Reproductive Endocrinology, Infertility, and Genetics, Department of Obstetrics and Gynecology, Institute of Molecular Medicine and Genetics, Neuroscience Program, Georgia Health Sciences University, Augusta, Georgia 30912, USA.

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http://dx.doi.org/10.1016/j.fertnstert.2011.09.046DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573697PMC
December 2011

Unique phenotype in a patient with CHARGE syndrome.

Int J Pediatr Endocrinol 2011 Oct 13;2011:11. Epub 2011 Oct 13.

State University of New York Downstate Medical Center, Children's Hospital at Downstate, Department of Pediatrics, Division of Pediatric Endocrinology, Brooklyn, NY 11203 USA.

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http://dx.doi.org/10.1186/1687-9856-2011-11DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3216247PMC
October 2011

The role of CHD7 and the newly identified WDR11 gene in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.

Mol Cell Endocrinol 2011 Oct 2;346(1-2):74-83. Epub 2011 Aug 2.

Section of Reproductive Endocrinology, Infertility, & Genetics, Department of Obstetrics & Gynecology, Georgia Health Sciences University, Augusta, GA 30912, United States.

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http://dx.doi.org/10.1016/j.mce.2011.07.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3924585PMC
October 2011

Rarer syndromes characterized by hypogonadotropic hypogonadism.

Front Horm Res 2010 8;39:154-167. Epub 2010 Apr 8.

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http://dx.doi.org/10.1159/000312701DOI Listing
December 2010

Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.

Am J Hum Genet 2008 Oct 2;83(4):511-9. Epub 2008 Oct 2.

Molecular Neurogenetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, and Department of Genetics, Harvard Medical School, Boston, MA 02114, USA.

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http://dx.doi.org/10.1016/j.ajhg.2008.09.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2561938PMC
October 2008

Clinical manifestations of impaired GnRH neuron development and function.

Neurosignals 2008 5;16(2-3):165-82. Epub 2008 Feb 5.

Department of Obstetrics and Gynecology, Institute of Molecular Medicine and Genetics, Medical College of Georgia, Augusta, GA 30912-3360, USA.

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http://dx.doi.org/10.1159/000111561DOI Listing
May 2008

Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann-Laband syndrome.

Am J Med Genet A 2007 Nov;143A(22):2668-74

Institut für Humangenetik, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.

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http://dx.doi.org/10.1002/ajmg.a.32034DOI Listing
November 2007

Candidate loci for Zimmermann-Laband syndrome at 3p14.3.

Am J Med Genet A 2007 Jan;143A(2):107-11

Molecular Neurogenetics Unit, Center for Human Genetic Research, Massachusetts General Hospital/Department of Genetics, Harvard Medical School, Boston, Massachusetts, USA.

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http://dx.doi.org/10.1002/ajmg.a.31544DOI Listing
January 2007

Gene expression profiling of the pre-implantation mouse embryo by microarray analysis: comparison of the two-cell stage and two-cell block.

Theriogenology 2006 Sep 13;66(4):785-96. Epub 2006 Jun 13.

Genome Research Center for Reproductive Medicine and Infertility of Korea, Ministry of Health & Welfare, Seoul 135-081, Republic of Korea.

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http://dx.doi.org/10.1016/j.theriogenology.2006.01.059DOI Listing
September 2006

Human chromosome 7: DNA sequence and biology.

Science 2003 May 10;300(5620):767-72. Epub 2003 Apr 10.

Department of Genetics and Genomic Biology, The Hospital for Sick Children, Toronto, Ontario, Canada, M5G 1X8.

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http://dx.doi.org/10.1126/science.1083423DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2882961PMC
May 2003