Roberts' ? SC phocomelia syndrome with cytogenetic findings
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00569225.pdf
Reference7 articles.
1. Freeman MVR, Williams DW, Schimke RN, Temtamy SA, Vachier E, German J (1974) The Roberts' syndrome. Clin Genet 5:1?16
2. German J (1979) Roberts' syndrome. I. Cytological evidence for a disturbance in chromatid pairing. Clin Genet 16:441?447
3. Herrmann J, Opitz JM (1977) The SC phocomelia and the Roberts syndrome: Nosologic aspects. Eur J Pediatr 125:117?134
4. Judge C (1973) A sibship with the pseudothalidomide syndrome and an association with Rh incompatibility. Med J Aust 2:280?281
5. Qazi QH, Kassner EG, Masakawa A, Madahar C, Choi SJ (1979) The SC phocomelia syndrome: Report of two cases with cytogenetic abnormality. Am J Med Genet 4:231?238
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1. Long‑term survival after corrective surgeries in two patients with severe deformities due to Roberts syndrome: A Case report and review of the literature;Experimental and Therapeutic Medicine;2017-12-05
2. Roberts syndrome and SC phocomelia. A single genetic entity;Clinical Genetics;2008-06-28
3. Roberts-Syndrom mit Aneurysma des interatrialen Septums, Kuhmilchproteinintoleranz und fehlendem Schluckreflex;Klinische Pädiatrie;1994-11
4. Clinical Heterogeneity of Skeletal Dysplasia in Roberts Syndrome: A Review;Human Heredity;1994
5. Roberts syndrome: A review of 100 cases and a new rating system for severity;American Journal of Medical Genetics;1993-11-15
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