Beyhan Tuysuz

Beyhan Tuysuz

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Beyhan Tuysuz

Publications by authors named "Beyhan Tuysuz"

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SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancy.

J Hum Genet 2019 Jul 24;64(7):609-616. Epub 2019 Apr 24.

Institut für Medizinische Genetik und Humangenetik, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.

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http://www.nature.com/articles/s10038-019-0602-8
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http://dx.doi.org/10.1038/s10038-019-0602-8DOI Listing
July 2019

A Novel Mutation of in a Child with 22q11.2 Deletion Syndrome Associated with MCLMR.

Mol Syndromol 2019 Jan 20;9(5):266-270. Epub 2018 Jul 20.

Department of Pediatric Genetics, Cerrahpaşa Medical Faculty, Istanbul University, Istanbul, Turkey.

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http://dx.doi.org/10.1159/000491568DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362857PMC
January 2019

Recessive MYF5 Mutations Cause External Ophthalmoplegia, Rib, and Vertebral Anomalies.

Am J Hum Genet 2018 07 7;103(1):115-124. Epub 2018 Jun 7.

Department of Neurology, Boston Children's Hospital, Boston, MA 02115, USA; F.M. Kirby Neurobiology Center, Boston Children's Hospital, Boston, MA 02115, USA; Department of Neurology, Harvard Medical School, Boston, MA 02115, USA; Broad Institute of M.I.T. and Harvard, Cambridge, MA 02142, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA; Department Ophthalmology, Boston Children's Hospital, Boston, MA 02115, USA; Department of Ophthalmology, Harvard Medical School, Boston, MA 02115, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2018.05.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6035164PMC
July 2018

Chromosome 14q11.2-q21.1 duplication: a rare cause of West syndrome.

Epileptic Disord 2018 Jun;20(3):219-224

Department of Pediatric Genetics, Cerrahpasa Faculty of Medicine, Istanbul University, Istanbul, Turkey.

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http://dx.doi.org/10.1684/epd.2018.0972DOI Listing
June 2018

Longitudinal Follow-Up of Two Patients with Dysspondyloenchondromatosis due to Novel Heterozygous Mutations in .

Mol Syndromol 2018 May 24;9(3):134-140. Epub 2018 Apr 24.

Department of Pediatric Genetics, Cerrahpaşa Medical School, Istanbul University, Istanbul, Turkey.

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http://dx.doi.org/10.1159/000488438DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006654PMC
May 2018

Mucolipidosis type III gamma: Three novel mutation and genotype-phenotype study in eleven patients.

Gene 2018 Feb 21;642:398-407. Epub 2017 Nov 21.

Department of Medical Genetics, BezmialemVakif University, Istanbul, Turkey.

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http://dx.doi.org/10.1016/j.gene.2017.11.052DOI Listing
February 2018

Two novel mutations in XYLT2 cause spondyloocular syndrome.

Am J Med Genet A 2017 Dec 8;173(12):3195-3200. Epub 2017 Sep 8.

Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden.

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http://dx.doi.org/10.1002/ajmg.a.38470DOI Listing
December 2017

A Novel de novo Mutation in a Patient with Autosomal Dominant Omodysplasia.

Mol Syndromol 2017 Nov 8;8(6):318-324. Epub 2017 Sep 8.

Department of Pediatric Genetics, Cerrahpaşa Medical School, Istanbul University, Istanbul, Turkey.

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http://dx.doi.org/10.1159/000479721DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701278PMC
November 2017

Follow-up Findings in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation in the GNAS Gene.

J Clin Res Pediatr Endocrinol 2017 Mar 18;9(1):74-79. Epub 2016 Jul 18.

İstanbul University Cerrahpaşa Faculty of Medicine, Department of Pediatric Genetics, İstanbul, Turkey Phone: +90 212 4143192 E-mail:

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http://dx.doi.org/10.4274/jcrpe.3191DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363169PMC
March 2017

Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum.

J Bone Miner Res 2016 08 4;31(8):1577-85. Epub 2016 Apr 4.

Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.

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http://dx.doi.org/10.1002/jbmr.2834DOI Listing
August 2016

Oral and craniofacial manifestations of Ellis-van Creveld syndrome: Case series.

J Craniomaxillofac Surg 2016 Aug 26;44(8):919-24. Epub 2016 Apr 26.

Istanbul University, Cerrahpasa Medical Faculty, Department of Pediatric Genetics, Istanbul, Turkey.

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http://dx.doi.org/10.1016/j.jcms.2016.04.025DOI Listing
August 2016

Natural History of Congenital Generalized Lipodystrophy: A Nationwide Study From Turkey.

J Clin Endocrinol Metab 2016 07 4;101(7):2759-67. Epub 2016 May 4.

Department of Internal Medicine (B.A., T.D., U.C., A.C.), Division of Endocrinology, Dokuz Eylul University, Izmir, Turkey; Department of Medical Genetics (H.O., S.O.), Ege University, Izmir, Turkey; Department of Pediatrics (S.O.), Division of Pediatric Endocrinology, Ege University, Izmir, Turkey; Department of Medical Genetics (H.K., U.A.), Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey; Department of Medical Genetics (H,K., A.A.), Koc University School of Medicine, Istanbul, Turkey; Division of Pediatric Neurology (G.A.), Dr. Behcet Uz Children's Hospital, Izmir, Turkey; Department of Pediatrics (B.N., E.M.), Division of Pediatric Genetics, Akdeniz University, Antalya, Turkey; Department of Pediatrics (B.T.), Division of Genetics, Istanbul Cerrahpasa University, Istanbul, Turkey; Division of Pediatric Endocrinology (M.N.O.), Diyarbakir Children's Hospital, Diyarbakir, Turkey; Department of Internal Medicine (A.G., H.B.S), Division of Endocrinology, Ataturk University, Erzurum, Turkey; Department of Internal Medicine (I.Y.S.), Division of Endocrinology, Ege University, Izmir, Turkey; Department of Radiology (C.A., M.S.), Dokuz Eylul University, Izmir, Turkey; Department of Biochemistry (L.D., F.S.), Ataturk Training Hospital, Izmir, Turkey; Department of Pediatrics (E.S.), Division of Pediatric Endocrinology, Osmangazi University, Eskisehir, Turkey; Department of Internal Medicine (M.A.), Division of Endocrinology, Yuzuncu Yil University, Van, Turkey; Department of Pediatrics (H.T.), Division of Pediatric Neurology, Hacettepe University, Ankara, Turkey; Department of Internal Medicine (H.A.), Division of Endocrinology, Ondokuz Mayis University, Samsun, Turkey; Department of Pediatrics (T.A.), Division of Pediatric Genetics, Ege University, Izmir, Turkey; and Department of Internal Medicine and the Center for Human Nutrition (A.G.), Division of Nutrition and Metabolic Diseases, UT Southwestern Medical Center, Dallas, Texas.

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http://dx.doi.org/10.1210/jc.2016-1005DOI Listing
July 2016

A patient with a novel homozygous missense mutation in FTO and concomitant nonsense mutation in CETP.

J Hum Genet 2016 May 7;61(5):395-403. Epub 2016 Jan 7.

Departments of Neurosurgery, Neurobiology and Genetics, Yale Program in Brain Tumor Research, Yale School of Medicine, New Haven, CT, USA.

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http://dx.doi.org/10.1038/jhg.2015.160DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4880488PMC
May 2016

Renal involvement in patients with mucolipidosis IIIalpha/beta: Causal relation or co-occurrence?

Am J Med Genet A 2016 May 8;170A(5):1187-95. Epub 2016 Jan 8.

Department of Neurosurgery, Program on Neurogenetics, Yale School of Medicine, New Haven, Connecticut.

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http://dx.doi.org/10.1002/ajmg.a.37543DOI Listing
May 2016

GORAB Missense Mutations Disrupt RAB6 and ARF5 Binding and Golgi Targeting.

J Invest Dermatol 2015 Oct 22;135(10):2368-2376. Epub 2015 May 22.

Institut fuer Medizinische Genetik und Humangenetik, Charité-Universitaetsmedizin Berlin, Berlin, Germany; Max-Planck-Institut fuer Molekulare Genetik, FG Development & Disease, Berlin, Germany; Berlin-Brandenburg Center for Regenerative Therapies (BCRT), Charité-Universitaetsmedizin Berlin, Berlin, Germany. Electronic address:

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http://dx.doi.org/10.1038/jid.2015.192DOI Listing
October 2015

Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene.

J Clin Res Pediatr Endocrinol 2015 Sep;7(3):242-8

İstanbul University Cerrahpaşa Faculty of Medicine, Department of Pediatric Endocrinology, İstanbul, Turkey Phone: +90 212 414 30 00 E-mail:

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http://dx.doi.org/10.4274/jcrpe.2067DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677562PMC
September 2015

A novel mutation in EED associated with overgrowth.

J Hum Genet 2015 Jun 19;60(6):339-42. Epub 2015 Mar 19.

1] Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada [2] Child and Family Research Institute, British Columbia Children's Hospital, Vancouver, BC, Canada.

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http://dx.doi.org/10.1038/jhg.2015.26DOI Listing
June 2015

Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type: longitudinal observation of radiographic findings in a child heterozygous for a KIF22 mutation.

Pediatr Radiol 2015 Apr 26;45(5):771-6. Epub 2014 Sep 26.

Department of Pediatric Genetics, Cerrahpaşa Medical School, Istanbul University, Cerrahpaşa Tıp Fakültesi, Çocuk kliniği, Cerrahpaşa, Istanbul, Turkey,

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http://link.springer.com/content/pdf/10.1007/s00247-014-3159
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http://link.springer.com/10.1007/s00247-014-3159-x
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http://dx.doi.org/10.1007/s00247-014-3159-xDOI Listing
April 2015

Primary hypertrophic osteoarthropathy caused by homozygous deletion in HPGD gene in a family: changing clinical and radiological findings with long-term follow-up.

Rheumatol Int 2014 Nov 12;34(11):1539-44. Epub 2014 May 12.

Department of Pediatric Genetics, Cerrahpaşa Medical School, Istanbul University, Istanbul, Turkey,

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http://dx.doi.org/10.1007/s00296-014-3037-8DOI Listing
November 2014

Hennekam syndrome can be caused by FAT4 mutations and be allelic to Van Maldergem syndrome.

Hum Genet 2014 Sep 7;133(9):1161-7. Epub 2014 Jun 7.

Department of Clinical Genetics, Academic Medical Centre, University of Amsterdam, Amsterdam, Netherlands.

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http://dx.doi.org/10.1007/s00439-014-1456-yDOI Listing
September 2014

Autosomal recessive spastic tetraplegia caused by AP4M1 and AP4B1 gene mutation: expansion of the facial and neuroimaging features.

Am J Med Genet A 2014 Jul 3;164A(7):1677-85. Epub 2014 Apr 3.

Department of Pediatric Genetics, Cerrahpaşa Medical School, Istanbul University, Istanbul, Turkey.

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http://dx.doi.org/10.1002/ajmg.a.36514DOI Listing
July 2014

Prevalence of Prader-Willi syndrome among infants with hypotonia.

J Pediatr 2014 May 25;164(5):1064-7. Epub 2014 Feb 25.

Department of Genetics, Institute for Experimental Medicine, Istanbul University, Istanbul, Turkey.

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http://dx.doi.org/10.1016/j.jpeds.2014.01.039DOI Listing
May 2014

XYLT1 mutations in Desbuquois dysplasia type 2.

Am J Hum Genet 2014 Mar 27;94(3):405-14. Epub 2014 Feb 27.

Department of Genetics, INSERM U781, Université Paris Descartes- Sorbonne Paris Cité, Institut Imagine, Hôpital Necker Enfants Malades (AP-HP), Paris 75015, France. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2014.01.020DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3951945PMC
March 2014

Spondyloepimetaphyseal dysplasia Pakistani type: expansion of the phenotype.

Am J Med Genet A 2013 Jun 30;161A(6):1300-8. Epub 2013 Apr 30.

Department of Pediatric Genetics, Cerrahpaşa Medical School, Istanbul University, Istanbul, Turkey.

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http://dx.doi.org/10.1002/ajmg.a.35906DOI Listing
June 2013

Macrocephaly-capillary malformation syndrome in a newborn with tetralogy of fallot and sagittal sinus thrombosis.

J Child Neurol 2013 Jan 25;28(1):115-9. Epub 2012 Mar 25.

Department of Neonatology, Cerrahpaşa Medical School, Istanbul University, Istanbul, Turkey.

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http://journals.sagepub.com/doi/10.1177/0883073812439346
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http://dx.doi.org/10.1177/0883073812439346DOI Listing
January 2013

First genetic screening for maternal uniparental disomy of chromosome 7 in Turkish silver-russell syndrome patients.

Iran J Pediatr 2012 Dec;22(4):445-51

Department of Genetics, Ege University Medical Faculty, Izmir, Turkey.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3533142PMC
December 2012

Growth charts of Turkish children with Down syndrome.

Am J Med Genet A 2012 Nov 5;158A(11):2656-64. Epub 2012 Oct 5.

Cerrahpasa Medical Faculty, Department of Pediatric Genetics, Istanbul University, Istanbul, Turkey.

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http://dx.doi.org/10.1002/ajmg.a.35710DOI Listing
November 2012

A microduplication of the Rubinstein-Taybi region on 16p13.3 in a girl with a bilateral complete cleft lip and palate and severe mental retardation.

Clin Dysmorphol 2012 Oct;21(4):204-7

Department of Pediatric Genetics, Cerrahpasa Medical Faculty, Istanbul University, Istanbul, Turkey.

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http://dx.doi.org/10.1097/MCD.0b013e3283554d15DOI Listing
October 2012

IMPAD1 mutations in two Catel-Manzke like patients.

Am J Med Genet A 2012 Sep 6;158A(9):2183-7. Epub 2012 Aug 6.

Département de génétique, Université Paris Descartes-Sorbonne Paris Cité, Institut Imagine, Hôpital Necker-Enfants Malades, Paris, France.

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http://dx.doi.org/10.1002/ajmg.a.35504DOI Listing
September 2012

A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?

Neuropediatrics 2012 Jun 19;43(3):159-61. Epub 2012 May 19.

Istanbul University, Cerrahpasa Medical Faculty, Department of Neurology, Division of Child Neurology, Istanbul, Turkey.

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http://dx.doi.org/10.1055/s-0032-1313912DOI Listing
June 2012

Mutations in the prostaglandin transporter encoding gene SLCO2A1 cause primary hypertrophic osteoarthropathy and isolated digital clubbing.

Hum Mutat 2012 Apr 24;33(4):660-4. Epub 2012 Feb 24.

Institute for Vegetative Anatomy, Charité-University Medicine of Berlin, Berlin, Germany.

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http://doi.wiley.com/10.1002/humu.22042
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http://dx.doi.org/10.1002/humu.22042DOI Listing
April 2012

Restrictive dermopathy in a Turkish newborn.

Pediatr Dermatol 2011 Jul-Aug;28(4):408-11. Epub 2010 Dec 2.

Cerrahpasa Medical Faculty, Department of Pediatric Genetics, Istanbul University, Istanbul, Turkey.

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http://dx.doi.org/10.1111/j.1525-1470.2010.01296.xDOI Listing
December 2011

Unilateral cerebellar hypoplasia with different clinical features.

Cerebellum 2011 Mar;10(1):49-60

Cerrahpasa Medical Faculty, Department of Neurology, Division of Pediatric Neurology, Istanbul University, Turkey.

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http://dx.doi.org/10.1007/s12311-010-0225-2DOI Listing
March 2011

The phenotype caused by PYCR1 mutations corresponds to geroderma osteodysplasticum rather than autosomal recessive cutis laxa type 2.

Am J Med Genet A 2011 Jan 9;155A(1):134-40. Epub 2010 Dec 9.

Department of Molecular Biology and Genetics, Boğaziçi University, Istanbul, Turkey.

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http://dx.doi.org/10.1002/ajmg.a.33747DOI Listing
January 2011

Four novel SCN1A mutations in Turkish patients with severe myoclonic epilepsy of infancy (SMEI).

J Child Neurol 2010 Oct 28;25(10):1265-8. Epub 2010 Jan 28.

Department of Neurosurgery, Yale University School of Medicine, New Haven, CT 06510, USA.

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http://dx.doi.org/10.1177/0883073809357241DOI Listing
October 2010

Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy.

Neurogenetics 2010 Jul 15;11(3):319-25. Epub 2010 Jan 15.

Department of Neurosurgery, Neurobiology, Program on Neurogenetics Yale University School of Medicine, New Haven, CT, USA.

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http://dx.doi.org/10.1007/s10048-009-0232-yDOI Listing
July 2010

Ocular manifestations of juvenile Paget disease.

Arch Ophthalmol 2010 Jun;128(6):698-703

Department of Ophthalmology, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.

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http://dx.doi.org/10.1001/archophthalmol.2010.76DOI Listing
June 2010

Mucolipidosis type IV in a Turkish boy associated with a novel MCOLN1 mutation.

Brain Dev 2009 Oct 8;31(9):702-5. Epub 2008 Nov 8.

Istanbul University, Cerrahpaşa Medical Faculty, Department of Pediatric Genetics, Istanbul, Turkey.

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http://dx.doi.org/10.1016/j.braindev.2008.10.001DOI Listing
October 2009

Clinical variability of Waardenburg-Shah syndrome in patients with proximal 13q deletion syndrome including the endothelin-B receptor locus.

Am J Med Genet A 2009 Oct;149A(10):2290-5

Department of Pediatric Genetics, Cerrahpaşa Medical Faculty, Istanbul University, Istanbul, Turkey.

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http://dx.doi.org/10.1002/ajmg.a.33031DOI Listing
October 2009

Clinical variability of asphyxiating thoracic dystrophy (Jeune) syndrome: Evaluation and classification of 13 patients.

Am J Med Genet A 2009 Aug;149A(8):1727-33

Department of Pediatric Genetics, Istanbul University, Turkey.

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http://dx.doi.org/10.1002/ajmg.a.32962DOI Listing
August 2009

A novel matrix metalloproteinase 2 (MMP2) terminal hemopexin domain mutation in a family with multicentric osteolysis with nodulosis and arthritis with cardiac defects.

Eur J Hum Genet 2009 May 5;17(5):565-72. Epub 2008 Nov 5.

Department of Pediatrics, Division of Genetics,Istanbul University Cerrahpasa Faculty of Medicine, Istanbul, Turkey.

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http://dx.doi.org/10.1038/ejhg.2008.204DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2721823PMC
May 2009

The time of onset of abnormal calcification in spondylometaepiphyseal dysplasia, short limb-abnormal calcification type.

Pediatr Radiol 2009 Jan 11;39(1):84-9. Epub 2008 Nov 11.

Department of Pediatric Genetics, Cerrahpaşa Medical School, Istanbul University, Istanbul, Turkey.

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http://link.springer.com/10.1007/s00247-008-1036-1
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http://dx.doi.org/10.1007/s00247-008-1036-1DOI Listing
January 2009

IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy.

Nat Genet 2007 Jun 29;39(6):727-9. Epub 2007 Apr 29.

Molecular Medicine Unit, University College London (UCL) Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK.

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http://dx.doi.org/10.1038/ng2038DOI Listing
June 2007

Detection of Y chromosomal material in patients with a 45,X karyotype by PCR method.

Tohoku J Exp Med 2007 Mar;211(3):243-9

Department of Medical Biology, Center for Genetic Diagnosis, School of Medicine, Pamukkale University, Denizli, Turkey.

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http://dx.doi.org/10.1620/tjem.211.243DOI Listing
March 2007

A new concept of skeletal dysplasias.

Authors:
Beyhan Tüysüz

Turk J Pediatr 2004 Jul-Sep;46(3):197-203

Division of Genetics, Department of Pediatrics, Istanbul University Cerrahpaşa Faculty of Medicine, Istanbul, Turkey.

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November 2004

Spondyloenchondrodysplasia: clinical variability in three cases.

Am J Med Genet A 2004 Jul;128A(2):185-9

Department of Pediatrics, Istanbul University, Cerrahpaşa Medical School, Istanbul, Turkey.

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http://doi.wiley.com/10.1002/ajmg.a.30078
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http://dx.doi.org/10.1002/ajmg.a.30078DOI Listing
July 2004

Congenital cutis laxa syndrome: type II autosomal recessive inheritance.

Turk J Pediatr 2003 Jul-Sep;45(3):265-8

Division of Genetics and Teratology, Department of Pediatrics, Istanbul University Cerrahpaşa Faculty of Medicine, Istanbul, Turkey.

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February 2004

Linear scleroderma en coup de sabre and brain calcification: is there a pathogenic relationship?

J Rheumatol 2003 Dec;30(12):2724-5; author reply 2725

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December 2003

Is the novel SCKL3 at 14q23 the predominant Seckel locus?

Eur J Hum Genet 2003 Nov;11(11):851-7

Department of Molecular Biology and Genetics, Bogaziçi University, Istanbul, Turkey.

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http://dx.doi.org/10.1038/sj.ejhg.5201057DOI Listing
November 2003

Short trunk stature, brachydactyly, and platyspondyly in three sibs: a new form of brachyolmia or a new skeletal dysplasia?

Am J Med Genet A 2003 Jun;119A(3):375-80

Department of Pediatrics, Cerrahpaşa Faculty of Medicine, Istanbul University, Istanbul, Turkey.

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http://doi.wiley.com/10.1002/ajmg.a.20125
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http://dx.doi.org/10.1002/ajmg.a.20125DOI Listing
June 2003

Abnormalities in the cerebral arterial system in osteogenesis imperfecta.

AJNR Am J Neuroradiol 2003 Apr;24(4):748-50

Department of Radiology, Division of Neuroradiology, Cerrahpasa Medical School, Istanbul University, Turkey.

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April 2003

Ankyloblepharon filiforme adnatum (AFA) associated with trisomy 18.

Turk J Pediatr 2002 Oct-Dec;44(4):360-2

Department of Pediatrics, Istanbul University Cerrahpaşa Faculty of Medicine, Istanbul, Turkey.

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February 2003

Patient with the mesomelic dysplasia, Nievergelt syndrome, and cerebellovermian agenesis and cataracts.

Am J Med Genet 2002 May;109(3):206-10

Division of Genetics and Teratology, Department of Pediatrics, University of Istanbul, Istanbul, Turkey.

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http://dx.doi.org/10.1002/ajmg.10283DOI Listing
May 2002

Prenatal diagnosis of arthrogryposis multiplex congenita with increased nuchal translucency but without any underlying fetal neurogenic or myogenic pathology.

Fetal Diagn Ther 2002 Jan-Feb;17(1):29-33

Department of Obstetrics and Gynaecology, Cerrahpasa Medical Faculty, University of Istanbul, Turkey.

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http://dx.doi.org/10.1159/000048002DOI Listing
April 2002