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22. Short stature, abnormal face, joint laxity, dislocation, hernias, delayed bone age, and severe psychomotor retardation in two brothers: previously undescribed MCA/MR syndrome. Mégarbané A, Ruchoux MM, Loeys B, Ayoub N, Nuytinck L. Am J Med Genet; 2001 Dec 01; 104(3):221-4. PubMed ID: 11754048 [Abstract] [Full Text] [Related]
23. [Simpson-Golabi-Behmel syndrome. A new overgrowth syndrome with increased risk of tumor development]. Weidle B, Orstavik KH. Tidsskr Nor Laegeforen; 1998 Apr 20; 118(10):1556-8. PubMed ID: 9615582 [Abstract] [Full Text] [Related]
26. Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome. Lin AE. Am J Med Genet; 1993 Jun 15; 46(5):606-7. PubMed ID: 8322829 [No Abstract] [Full Text] [Related]
38. [A casuistic contribution to potter syndrome of dysplasia renofacialis with and without sirenomelia (author's transl)]. Kühner U, Buchinger G, Fricke G, Romen H. Klin Padiatr; 1976 May 24; 188(3):289-94. PubMed ID: 945426 [Abstract] [Full Text] [Related]
39. Roberts syndrome: study of 4 new Rgyptian cases with comparison of clinical and cytogenetic findings. Temtamy SA, Ismail S, Helmy NA. Genet Couns; 2006 May 24; 17(1):1-13. PubMed ID: 16719272 [Abstract] [Full Text] [Related]
40. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome? Bindewald B, Ulmer H, Müller U. Am J Med Genet; 1994 Apr 01; 50(2):173-6. PubMed ID: 8010348 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]