Taosheng Huang

Taosheng Huang

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Taosheng Huang

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Mitochondria and Their Role in Human Reproduction.

DNA Cell Biol 2019 Oct 11. Epub 2019 Oct 11.

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.

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http://dx.doi.org/10.1089/dna.2019.4807DOI Listing
October 2019

Reply to Annis et al.: Is quasi-Mendelian mtDNA competition enough to drive transmission of paternal mtDNA?

Proc Natl Acad Sci U S A 2019 Jul 16;116(30):14799-14800. Epub 2019 Jul 16.

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229;

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http://dx.doi.org/10.1073/pnas.1909445116DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6660767PMC
July 2019

Mitochondrial DNA Variants and Common Diseases: A Mathematical Model for the Diversity of Age-Related mtDNA Mutations.

Cells 2019 06 18;8(6). Epub 2019 Jun 18.

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.

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http://dx.doi.org/10.3390/cells8060608DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627076PMC
June 2019

A rapid bioanalytical tool for detection of sequence-specific circular DNA and mitochondrial DNA point mutations.

Anal Bioanal Chem 2019 Apr 27;411(10):1935-1941. Epub 2019 Feb 27.

Department of Electrical Engineering and Computer Science, University of Cincinnati, Cincinnati, OH, 45221, USA.

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http://dx.doi.org/10.1007/s00216-019-01683-8DOI Listing
April 2019

[The history and current status of medical genetics and genomics system in the United States].

Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2019 Jan;36(1):1-6

Department of Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.

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http://dx.doi.org/10.3760/cma.j.issn.1003-9406.2019.01.001DOI Listing
January 2019

65 YEARS OF THE DOUBLE HELIX: The advancements of gene editing and potential application to hereditary cancer.

Endocr Relat Cancer 2018 08;25(8):T141-T158

Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore

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http://dx.doi.org/10.1530/ERC-18-0039DOI Listing
August 2018

Validation of the diagnostic potential of mtDNA copy number derived from whole genome sequencing.

J Genet Genomics 2018 Jun 6. Epub 2018 Jun 6.

Division of Human Genetics, Children's Hospital Medical Center, Cincinnati, OH 45229, USA; Human Aging Research Institute, Nanchang University, Nanchang 330031, China. Electronic address:

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http://dx.doi.org/10.1016/j.jgg.2018.06.001DOI Listing
June 2018

A Multiplex Asymmetric Reverse Transcription-PCR Assay Combined With an Electrochemical DNA Sensor for Simultaneously Detecting and Subtyping Influenza A Viruses.

Front Microbiol 2018 27;9:1405. Epub 2018 Jun 27.

Beijing Key Laboratory of Pediatric Respiratory Infection Diseases, Key Laboratory of Major Diseases in Children, Ministry of Education, National Clinical Research Center for Respiratory Diseases, National Key Discipline of Pediatrics (Capital Medical University), Beijing Pediatric Research Institute, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.

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http://dx.doi.org/10.3389/fmicb.2018.01405DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6036258PMC
June 2018

The current landscape for the treatment of mitochondrial disorders.

J Genet Genomics 2018 02 14;45(2):71-77. Epub 2018 Feb 14.

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA; Human Aging Research Institute, Nanchang University, Nanchang 330031, China. Electronic address:

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http://dx.doi.org/10.1016/j.jgg.2017.11.008DOI Listing
February 2018

Novel Mutations in EPCAM Cause Congenital Tufting Enteropathy.

J Clin Gastroenterol 2018 Jan;52(1):e1-e6

Department of Gastroenterology, Children's Hospital of Fudan University, Shanghai.

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http://dx.doi.org/10.1097/MCG.0000000000000739DOI Listing
January 2018

Corrigendum to 'Live birth derived from oocyte spindle transfer to prevent mitochondrial disease': [Reproductive BioMedicine Online 34 (2017) 361-368].

Reprod Biomed Online 2017 12 20;35(6):750. Epub 2017 Jul 20.

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA. Electronic address:

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http://dx.doi.org/10.1016/j.rbmo.2017.07.008DOI Listing
December 2017

Response: First birth following spindle transfer - should we stay or should we go?

Reprod Biomed Online 2017 11 12;35(5):546-547. Epub 2017 Jul 12.

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.

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http://dx.doi.org/10.1016/j.rbmo.2017.07.004DOI Listing
November 2017

Perspective: Is Random Monoallelic Expression a Contributor to Phenotypic Variability of Autosomal Dominant Disorders?

Front Genet 2017 29;8:191. Epub 2017 Nov 29.

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.

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http://dx.doi.org/10.3389/fgene.2017.00191DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5718016PMC
November 2017

Corrigendum to 'Live birth derived from oocyte spindle transfer to prevent mitochondrial disease' [Reproductive BioMedicine Online 34 (2017) 361-368].

Reprod Biomed Online 2017 07 8;35(1):49. Epub 2017 May 8.

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA. Electronic address:

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http://dx.doi.org/10.1016/j.rbmo.2017.04.002DOI Listing
July 2017

Live birth derived from oocyte spindle transfer to prevent mitochondrial disease.

Reprod Biomed Online 2017 04;34(4):361-368

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA. Electronic address:

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http://dx.doi.org/10.1016/j.rbmo.2017.01.013DOI Listing
April 2017

The Phosphatidylcholine Transfer Protein Stard7 is Required for Mitochondrial and Epithelial Cell Homeostasis.

Sci Rep 2017 04 12;7:46416. Epub 2017 Apr 12.

Perinatal Institute, Division of Neonatology, Perinatal and Pulmonary Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229-3039, USA.

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http://dx.doi.org/10.1038/srep46416DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388865PMC
April 2017

A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function.

Nucleic Acids Res 2016 12 17;44(22):10974-10985. Epub 2016 Aug 17.

Division of Clinical Genetics and Genomics, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310058, China

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http://dx.doi.org/10.1093/nar/gkw726DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5159531PMC
December 2016

Age-Related Accumulation of Somatic Mitochondrial DNA Mutations in Adult-Derived Human iPSCs.

Cell Stem Cell 2016 05 14;18(5):625-36. Epub 2016 Apr 14.

Center for Embryonic Cell and Gene Therapy, Oregon Health & Science University, 3303 SW Bond Avenue, Portland, OR 97239, USA; Division of Reproductive and Developmental Sciences, Oregon National Primate Research Center, Oregon Health & Science University, 505 NW 185th Avenue, Beaverton, OR 97006, USA; Department of Molecular and Medical Genetics, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239, USA; Division of Reproductive Endocrinology, Department of Obstetrics and Gynecology, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239, USA; Knight Cardiovascular Institute, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239, USA; Department of Biomedical Engineering, Oregon Health & Science University, 3303 SW Bond Avenue, Portland, OR 97239, USA. Electronic address:

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http://dx.doi.org/10.1016/j.stem.2016.02.005DOI Listing
May 2016

Neonatal multiorgan failure due to ACAD9 mutation and complex I deficiency with mitochondrial hyperplasia in liver, cardiac myocytes, skeletal muscle, and renal tubules.

Hum Pathol 2016 Mar 28;49:27-32. Epub 2015 Oct 28.

Divisions of Human Genetics, Gastroenterology, and Pathology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229. Electronic address:

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http://dx.doi.org/10.1016/j.humpath.2015.09.039DOI Listing
March 2016

The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.

Hum Mol Genet 2016 Feb 8;25(3):584-96. Epub 2015 Dec 8.

Institute of Genetics, Zhejiang University, School of Medicine, Hangzhou, Zhejiang, China, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Zhejiang University, Hangzhou, China,

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http://dx.doi.org/10.1093/hmg/ddv498DOI Listing
February 2016

Modeling autosomal dominant optic atrophy using induced pluripotent stem cells and identifying potential therapeutic targets.

Stem Cell Res Ther 2016 Jan 7;7. Epub 2016 Jan 7.

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA.

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http://dx.doi.org/10.1186/s13287-015-0264-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4704249PMC
January 2016

Phenotypic and functional characterization of Bst+/- mouse retina.

Dis Model Mech 2015 Aug 8;8(8):969-76. Epub 2015 May 8.

Department of Pediatrics, Division of Human Genetics, University of California, Irvine, CA 92697, USA Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA

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http://dx.doi.org/10.1242/dmm.018176DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4527279PMC
August 2015

Metabolic rescue in pluripotent cells from patients with mtDNA disease.

Nature 2015 Aug 15;524(7564):234-8. Epub 2015 Jul 15.

1] Center for Embryonic Cell and Gene Therapy, Oregon Health &Science University, 3303 S.W. Bond Avenue, Portland, Oregon 97239, USA [2] Division of Reproductive &Developmental Sciences, Oregon National Primate Research Center, Oregon Health &Science University, 505 N.W. 185th Avenue, Beaverton, Oregon 97006, USA.

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http://dx.doi.org/10.1038/nature14546DOI Listing
August 2015

Prevalence of Mitochondrial ND4 Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy.

Invest Ophthalmol Vis Sci 2015 Jul;56(8):4778-88

Institute of Genetics, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China 2Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Zhejiang University, Hangzhou, China 8Division of Human Genetics, Cincinnati Chi.

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http://dx.doi.org/10.1167/iovs.14-16158DOI Listing
July 2015

A deafness-associated tRNAHis mutation alters the mitochondrial function, ROS production and membrane potential.

Nucleic Acids Res 2014 Jul 11;42(12):8039-48. Epub 2014 Jun 11.

Institute of Genetics, Zhejiang University, Hangzhou, Zhejiang, China 310058 Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA 45229

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http://dx.doi.org/10.1093/nar/gku466DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4081083PMC
July 2014

Chemically induced specification of retinal ganglion cells from human embryonic and induced pluripotent stem cells.

Stem Cells Transl Med 2014 Apr 3;3(4):424-32. Epub 2014 Feb 3.

Department of Pediatrics, Division of Human Genetics, Department of Anatomy and Neurobiology, Department of Psychiatry and Human Behavior, MitoMed Molecular Diagnostic Laboratory, Department of Pathology, Department of Developmental and Cell Biology, and Department of Ophthalmology, University of California, Irvine, Irvine, California, USA; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.

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http://dx.doi.org/10.5966/sctm.2013-0147DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973714PMC
April 2014

Species identification through mitochondrial rRNA genetic analysis.

Sci Rep 2014 Feb 13;4:4089. Epub 2014 Feb 13.

1] Division of Human Genetics, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229 [2] Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45229.

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http://dx.doi.org/10.1038/srep04089DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379257PMC
February 2014

Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families.

Mitochondrion 2013 Nov 9;13(6):772-81. Epub 2013 May 9.

Department of Genetics, College of Life Sciences, Zhejiang University, Hangzhou, Zhejiang, China; School of Ophthalmology and Optometry, Wenzhou Medical College, Wenzhou, Zhejiang, China; Attardi Institute of Mitochondrial Biomedicine, Wenzhou Medical College, Wenzhou, Zhejiang, China.

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http://dx.doi.org/10.1016/j.mito.2013.05.002DOI Listing
November 2013

A Novel Exonic Splicing Mutation in the TAZ (G4.5) Gene in a Case with Atypical Barth Syndrome.

JIMD Rep 2013 19;11:99-106. Epub 2013 Apr 19.

John Welsh Cardiovascular Diagnostic Laboratory, Section of Cardiology, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.

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http://dx.doi.org/10.1007/8904_2013_228DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3755548PMC
August 2013

TBX3 promotes human embryonic stem cell proliferation and neuroepithelial differentiation in a differentiation stage-dependent manner.

Stem Cells 2012 Oct;30(10):2152-63

Department of Pediatrics, Division of Human Genetics, University of California, Irvine, California 92697, USA.

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http://doi.wiley.com/10.1002/stem.1187
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http://dx.doi.org/10.1002/stem.1187DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3517731PMC
October 2012

The spectrum of 4q- syndrome illustrated by a case series.

Gene 2012 Sep 3;506(2):387-91. Epub 2012 Jul 3.

Institute of Human Genetics and Newcastle University, Newcastle upon Tyne, UK.

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http://dx.doi.org/10.1016/j.gene.2012.06.087DOI Listing
September 2012

Next generation sequencing to characterize mitochondrial genomic DNA heteroplasmy.

Authors:
Taosheng Huang

Curr Protoc Hum Genet 2011 Oct;Chapter 19:Unit19.8

Division of Human Genetics/Department of Pediatrics, Center for Molecular and Mitochondrial Medicine and Genetics, University of California, Irvine, Irvine, California, USA.

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http://dx.doi.org/10.1002/0471142905.hg1908s71DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4687495PMC
October 2011

Left ventricular noncompaction is associated with mutations in the mitochondrial genome.

Mitochondrion 2010 Jun 6;10(4):350-7. Epub 2010 Mar 6.

Division of Human Genetics/Department of Pediatrics, University of California, Irvine, CA 92697, United States.

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http://dx.doi.org/10.1016/j.mito.2010.02.003DOI Listing
June 2010

Genotyping mitochondrial DNA single nucleotide polymorphisms by PCR ligase detection reactions.

Clin Chem Lab Med 2010 Apr;48(4):475-83

Department of Pathophysiology and High Altitude Physiology, Third Military Medical University, Chongqing, PR China.

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http://dx.doi.org/10.1515/CCLM.2010.097DOI Listing
April 2010

Characterization of mitochondrial DNA heteroplasmy using a parallel sequencing system.

Biotechniques 2010 Apr;48(4):287-96

Division of Human Genetics/Department of Pediatrics, University of California, Irvine, CA 92697, USA.

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http://dx.doi.org/10.2144/000113389DOI Listing
April 2010

Mutation of OPA1 gene causes deafness by affecting function of auditory nerve terminals.

Brain Res 2009 Dec 3;1300:97-104. Epub 2009 Sep 3.

Department of Pediatrics, University of California, Irvine, CA, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S000689930901809
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http://dx.doi.org/10.1016/j.brainres.2009.08.083DOI Listing
December 2009

Heterozygous mutation of Opa1 in Drosophila shortens lifespan mediated through increased reactive oxygen species production.

PLoS One 2009 16;4(2):e4492. Epub 2009 Feb 16.

Division of Human Genetics, Department of Pediatrics, University of California Irvine, Irvine, California, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0004492PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2637430PMC
April 2009

Mitochondrial genome analysis of Ochotona curzoniae and implication of cytochrome c oxidase in hypoxic adaptation.

Mitochondrion 2008 Dec 3;8(5-6):352-7. Epub 2008 Aug 3.

Department of Pathophysiology and High Altitude Physiology, College of High Altitude Medicine, Third Military Medical University, Chongqing 400038, China.

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http://linkinghub.elsevier.com/retrieve/pii/S156772490800060
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http://dx.doi.org/10.1016/j.mito.2008.07.005DOI Listing
December 2008

TBX3 is overexpressed in breast cancer and represses p14 ARF by interacting with histone deacetylases.

Cancer Res 2008 Feb;68(3):693-9

Department of Pediatrics, Division of Human Genetics, University of California, Irvine, California 92697, USA.

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http://cancerres.aacrjournals.org/cgi/doi/10.1158/0008-5472.
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http://dx.doi.org/10.1158/0008-5472.CAN-07-5012DOI Listing
February 2008

A novel RUNX2 missense mutation predicted to disrupt DNA binding causes cleidocranial dysplasia in a large Chinese family with hyperplastic nails.

BMC Med Genet 2007 Dec 31;8:82. Epub 2007 Dec 31.

The prenatal diagnostic Center of Wenzhou City, Department of genetics of Wenzhou No2 Hospital, Wenzhou, China.

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http://dx.doi.org/10.1186/1471-2350-8-82DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2241583PMC
December 2007

TBX3 and its isoform TBX3+2a are functionally distinctive in inhibition of senescence and are overexpressed in a subset of breast cancer cell lines.

Cancer Res 2004 Aug;64(15):5132-9

Division of Genetics, Department of Pediatrics, Robert R. Sprague Hall 314, University of California-Irvine, Irvine, CA 92697, USA.

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http://dx.doi.org/10.1158/0008-5472.CAN-04-0615DOI Listing
August 2004

Unilateral transverse arm defect with subterminal digital nubbins.

Pediatr Dev Pathol 2003 Jul-Aug;6(4):348-54

Department of Pathology, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, USA.

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May 2004

TBX5, a gene mutated in Holt-Oram syndrome, is regulated through a GC box and T-box binding elements (TBEs).

J Cell Biochem 2004 May;92(1):189-99

Department of Pediatrics, Division of Human Genetics and Metabolism, University of California, Irvine, California 92697, USA.

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http://dx.doi.org/10.1002/jcb.20039DOI Listing
May 2004

Identification of the TBX5 transactivating domain and the nuclear localization signal.

Gene 2004 Apr;330:9-18

Department of Pediatrics, Division of Human Genetics, University of California, Irvine, CA 92697, USA.

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http://dx.doi.org/10.1016/j.gene.2004.01.017DOI Listing
April 2004

Multiple congenital anomalies associated with in utero exposure of phenytoin: possible hypoxic ischemic mechanism?

Birth Defects Res A Clin Mol Teratol 2003 Dec;67(12):993-6

Children's Hospital, Boston, Massachusetts, USA.

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http://dx.doi.org/10.1002/bdra.10100DOI Listing
December 2003

Cardiac phenotypes in chromosome 4q- syndrome with and without a deletion of the dHAND gene.

Genet Med 2002 Nov-Dec;4(6):464-7

Division of Genetics, Department of Pediatrics, University California, Irvine, California 92697, USA.

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http://dx.doi.org/10.109700125817-200211000-00011DOI Listing
May 2003

Current advances in Holt-Oram syndrome.

Authors:
Taosheng Huang

Curr Opin Pediatr 2002 Dec;14(6):691-5

Division of Human Genetics, Department of Pediatrics, Unversity of California, Irvine, California 92697, USA.

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http://dx.doi.org/10.1097/00008480-200212000-00008DOI Listing
December 2002

Four cases with hypoplastic thumbs and encephaloceles.

Am J Med Genet 2002 Aug;111(2):178-81

Division of Genetics and Metabolism, Children's Hospital, Boston, Massachusetts, USA.

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http://dx.doi.org/10.1002/ajmg.10439DOI Listing
August 2002