Agenesis of the corpus callosum in Schinzel-Giedion syndrome associated with 47, XXY karyotype
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1996.tb02369.x/fullpdf
Reference11 articles.
1. The Schinzel-Giedion syndrome;Al-Gazali;J Med Genet,1990
2. A further case of a new syndrome including midface retraction, hypertrichosis, and skeletal anomalies;Donnai;J Med Genet,1979
3. Schinzel-Giedion syndrome and congenital megacalyces;Herman;Pediatr Radiol,1993
4. Congenital hydronephrosis, skeletal dysplasia, and severe developmental retardation: the Schinzel-Giedion syndrome;Kelley;J Pediatr,1982
5. Ultrasonic evaluation of fetal kidneys;Lawson;Radiology,1981
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1. Klinefelter Syndrome and Corpus Callosum Agenesis;The Indian Journal of Pediatrics;2020-05-08
2. Schinzel–Giedion syndrome: a novel case, review and revised diagnostic criteria;Journal of Genetics;2018-01-29
3. Schinzel-Giedion syndrome in two Brazilian patients: Report of a novel mutation inSETBP1and literature review of the clinical features;American Journal of Medical Genetics Part A;2015-02-07
4. Cobblestone Lissencephaly in Schinzel-Giedion Syndrome;Journal of Child Neurology;2012-04-24
5. Scoliosis in a Case of Schinzel–Giedion Syndrome;HSS Journal®: The Musculoskeletal Journal of Hospital for Special Surgery;2009-09
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