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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

404 related items for PubMed ID: 8287191

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  • 2. [Ectrodactyly, ectodermal dysplasia, and cleft lip and palate: an hereditary syndrome with an autosomal dominant mode of inheritance (author's transl)].
    Pfeiffer RA, Verbeck C.
    Z Kinderheilkd; 1973 Oct 01; 115(3):235-44. PubMed ID: 4801123
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  • 5. Untreated growth hormone deficiency with extremely short stature, bone dysplasia, cleft lip--palate and severe mental retardation in a 26-year-old man with a de novo unbalanced translocation t(1;12)(q24;q24).
    Callier P, Faivre L, Marle N, Thauvin-Robinet C, Mosca AL, Masurel-Paulet A, Borgnon J, Falcon-Eicher S, Danino A, Malka G, Le Merrer M, Huet F, Mugneret F.
    Eur J Med Genet; 2007 Oct 01; 50(6):455-64. PubMed ID: 17720646
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  • 6. Duplication of (2)(q11.1-q13.2) in a boy with mental retardation and cleft lip and palate: another clefting gene locus on proximal 2q?
    Riegel M, Schinzel A.
    Am J Med Genet; 2002 Jul 22; 111(1):76-80. PubMed ID: 12124740
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  • 7. [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
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  • 8. 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
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  • 9. Terminal deletion 6p23: a case report.
    Kormann-Bortolotto MH, Farah LM, Soares D, Corbani M, Müller R, Adell AC.
    Am J Med Genet; 1990 Dec 30; 37(4):475-7. PubMed ID: 2260591
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  • 10. Association of autosomal dominant cleft lip and palate and translocation 6p23;9q22.3.
    Donnai D, Heather LJ, Sinclair P, Thakker Y, Scambler PJ, Dixon MJ.
    Clin Dysmorphol; 1992 Apr 30; 1(2):89-97. PubMed ID: 1345518
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  • 13. Van der Woude syndrome with mental retardation: case report.
    Ugwu BT, Momoh JT.
    East Afr Med J; 2001 Feb 30; 78(2):111-2. PubMed ID: 11682943
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  • 14. [Ectrodactyly, ectodermal dysplasia, cleft lip and palate syndrome (EEC syndrome)].
    Ostorharics-Horváth G, Lázár I.
    Orv Hetil; 1989 Oct 08; 130(41):2211-2. PubMed ID: 2812754
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  • 16. Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance.
    Camera G, Centa A, Pozzolo S, Camera A.
    Clin Dysmorphol; 1993 Oct 08; 2(4):317-21. PubMed ID: 8305962
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  • 17. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomalies.
    Malpuech G, Demeocq F, Palcoux JB, Vanlieferinghen P.
    Am J Med Genet; 1983 Dec 08; 16(4):475-80. PubMed ID: 6660246
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  • 18. Ectrodactyly and proximal/intermediate interstitial deletion 7q.
    McElveen C, Carvajal MV, Moscatello D, Towner J, Lacassie Y.
    Am J Med Genet; 1995 Mar 13; 56(1):1-5. PubMed ID: 7747769
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  • 19. 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
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