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4. Feingold syndrome: report of a new family and review. Courtens W, Levi S, Verbelen F, Verloes A, Vamos E. Am J Med Genet; 1997 Nov 28; 73(1):55-60. PubMed ID: 9375923 [Abstract] [Full Text] [Related]
6. Vertebral anomalies in a new family with ODED syndrome. Piersall LD, Dowton SB, McAlister WH, Waggoner DJ. Clin Genet; 2000 Jun 28; 57(6):444-8. PubMed ID: 10905665 [Abstract] [Full Text] [Related]
7. A Feingold syndrome case with previously undescribed features and a new mutation. Koçak H, Ozaydin E, Köse G, Marcelis CL, Kamsteeg EJ, Ceylaner S. Genet Couns; 2009 Jun 28; 20(3):261-7. PubMed ID: 19852433 [Abstract] [Full Text] [Related]
8. How many entities exist for the spectrum of disorders associated with brachydactyly, syndactyly, short stature, microcephaly, and intellectual disability? Ravel A, Chouery E, Stora S, Jalkh N, Villard L, Temtamy S, Mégarbané A. Am J Med Genet A; 2011 Apr 28; 155A(4):880-4. PubMed ID: 21416592 [Abstract] [Full Text] [Related]
10. Distal aphalangia, syndactyly, and extra metatarsal, associated with short stature, microcephaly, and borderline intelligence: a new autosomal dominant disorder. Martínez-Frías ML, Martín M, Pardo M, Fernandez de las Heras F, Frías JL. Am J Med Genet; 1995 Jan 16; 55(2):213-6. PubMed ID: 7717420 [Abstract] [Full Text] [Related]
11. Total anonychia congenita and microcephaly with normal intelligence: a new autosomal-recessive syndrome? Teebi AS, Kaurah P. Am J Med Genet; 1996 Dec 18; 66(3):257-60. PubMed ID: 8985482 [Abstract] [Full Text] [Related]
12. Imperforate anus in Feingold syndrome. Büttiker V, Wojtulewicz J, Wilson M. Am J Med Genet; 2000 May 29; 92(3):166-9. PubMed ID: 10817649 [Abstract] [Full Text] [Related]
16. Microcephaly with large anterior fontanelle, generalized convulsions, micropenis, and distinct anomalies of the hands and feet. Another example of Wiedemann syndrome? Nevin NC, Stewart FJ, Corkey CW, Bell BA. Clin Genet; 1994 Aug 29; 46(2):205-8. PubMed ID: 7529662 [Abstract] [Full Text] [Related]
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20. Anonychia and absence/hypoplasia of distal phalanges (Cooks syndrome): report of a second family. Nevin NC, Thomas PS, Eedy DJ, Shepherd C. J Med Genet; 1995 Aug 29; 32(8):638-41. PubMed ID: 7473658 [Abstract] [Full Text] [Related] Page: [Next] [New Search]