Genome wide analysis in a discordant monozygotic twin with caudal appendage and multiple congenital anomalies.

Özgür Çoğulu(Ege University), Ferda Özkınay(Ege University), Nilgün Kültürsay, Erhan Parıltay(Ege University), E Levent(Ege University), R Ozyurek, Ayça Aykut(Ege University), Özge Altun Köroğlu

PubMed

January 1, 2013

Cited by 2

Related Papers

SMOC1 Is Essential for Ocular and Limb Development in Humans and Mice

|The American Journal of Human Genetics|2010|118

The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

|Journal of Human Genetics|2014|54

Demographic, clinical, and laboratory features of COVID‐19 in children: The role of mean platelet volume in predicting hospitalization and severity

|Journal of Medical Virology|2021|53

Single center experience of biotinidase deficiency: 259 patients and six novel mutations

|Journal of Pediatric Endocrinology and Metabolism|2018|37

DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo

|Brazilian Journal of Psychiatry|2020|33