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Journal Abstract Search
735 related items for PubMed ID: 8737656
1. Ectodermal dysplasia, Rapp-Hodgkin type in a mother and severe ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) in her child. Moerman P, Fryns JP. Am J Med Genet; 1996 Jun 14; 63(3):479-81. PubMed ID: 8737656 [Abstract] [Full Text] [Related]
6. Genitourinary anomalies are a component manifestation in the ectodermal dysplasia, ectrodactyly, cleft lip/palate (EEC) syndrome. Rollnick BR, Hoo JJ. Am J Med Genet; 1988 Jan 14; 29(1):131-6. PubMed ID: 3278611 [Abstract] [Full Text] [Related]
7. [Dysmaturity as symptom of the ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome]. Porcelijn L, Maat-Kievit JA, van Haeringen A. Tijdschr Kindergeneeskd; 1993 Jun 14; 61(3):96-9. PubMed ID: 8211943 [Abstract] [Full Text] [Related]
9. A novel H208D TP63 mutation in a familial case of ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome without clefting. Sorasio L, Biamino E, Garelli E, Ferrero GB, Silengo MC. Clin Exp Dermatol; 2009 Dec 14; 34(8):e726-8. PubMed ID: 19663851 [Abstract] [Full Text] [Related]
10. Adipsic hypernatremia and bilateral renal stones in a child with ectrodactyly-ectodermal dysplasia-cleft lip-palate (EEC) syndrome. Shawky RM, Elsayed SM, Sadik DI, Gad S, Seifeldin NS. Genet Couns; 2010 Dec 14; 21(2):215-20. PubMed ID: 20681222 [Abstract] [Full Text] [Related]
11. Ectodermal dysplasia, ectrodactyly, cleft lip/palate syndrome without ectrodactyly. Sankhyan N, Kaushal RK, Sarin S. Dermatol Online J; 2006 May 30; 12(4):5. PubMed ID: 17083860 [Abstract] [Full Text] [Related]
12. [Familial split hand and foot, cleft lip and palate, ectodermal dysplasia syndrome]. Szappanos L, Czeizel E, Szepesi K. Orv Hetil; 1984 Mar 11; 125(11):633-8. PubMed ID: 6700970 [No Abstract] [Full Text] [Related]
13. Ectrodactary, ectodermal dysplasia, and cleft lip-palate syndrome. Choong YY, Norazlina B. Med J Malaysia; 2001 Mar 11; 56(1):88-91. PubMed ID: 11503303 [Abstract] [Full Text] [Related]
14. De novo missense mutation, S541Y, in the p63 gene underlying Rapp-Hodgkin ectodermal dysplasia syndrome. Shotelersuk V, Janklat S, Siriwan P, Tongkobpetch S. Clin Exp Dermatol; 2005 May 11; 30(3):282-5. PubMed ID: 15807690 [Abstract] [Full Text] [Related]
16. Rapp-Hodgkin syndrome: report of a Brazilian family. Rodini EO, Freitas JA, Richieri-Costa A. Am J Med Genet; 1990 Aug 11; 36(4):463-6. PubMed ID: 2389804 [Abstract] [Full Text] [Related]
18. R298Q mutation of p63 gene in autosomal dominant ectodermal dysplasia associated with arrhythmogenic right ventricular cardiomyopathy. Valenzise M, Arrigo T, De Luca F, Privitera A, Frigiola A, Carando A, Garelli E, Silengo M. Eur J Med Genet; 2008 Aug 11; 51(5):497-500. PubMed ID: 18603493 [Abstract] [Full Text] [Related]
19. EC syndrome in a girl with paracentric inversion (7)(q22.1;q36.3). Akita S, Kuratomi H, Abe K, Harada N, Mukae N, Niikawa N. Clin Dysmorphol; 1993 Jan 11; 2(1):62-7. PubMed ID: 8298740 [Abstract] [Full Text] [Related]