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Results 1 - 10 of 55 for christian syndrome
  1. Lacrimo-auriculo-dento-digital syndrome 
    ... 38(4):495. Kubisch, Chriutian [corrected to Kubisch, Christian]. Citation on PubMed
    https://medlineplus.gov/.../lacrimo-auriculo-dento-digital-syndrome - Genetics
  2. FGFR2 gene 
    ... 38(4):495. Kubisch, Chriutian [corrected to Kubisch, Christian]. Citation on PubMed Shams I, Rohmann E, Eswarakumar VP, Lew ED, Yuzawa S, Wollnik B, Schlessinger J, Lax I. Lacrimo-auriculo-dento-digital syndrome is caused by reduced activity of the fibroblast ...
    https://medlineplus.gov/genetics/gene/fgfr2 - Genetics
  3. FGF10 gene 
    ... 38(4):495. Kubisch, Chriutian [corrected to Kubisch, Christian]. Citation on PubMed Shams I, Rohmann E, Eswarakumar VP, Lew ED, Yuzawa S, Wollnik B, Schlessinger J, Lax I. Lacrimo-auriculo-dento-digital syndrome is caused by reduced activity of the fibroblast ...
    https://medlineplus.gov/genetics/gene/fgf10 - Genetics
  4. UBE3A gene 
    ... Tsai TF, Matsuura T, Benton CS, Sutcliffe JS, Christian SL, Kubota T, Halley DJ, Meijers-Heijboer H, Langlois S, Graham JM Jr, Beuten J, Willems PJ, Ledbetter DH, Beaudet AL. The spectrum of mutations in UBE3A causing Angelman syndrome. Hum Mol Genet. 1999 Jan;8(1):129- ...
    https://medlineplus.gov/genetics/gene/ube3a - Genetics
  5. FGFR3 gene 
    ... 38(4):495. Kubisch, Chriutian [corrected to Kubisch, Christian]. Citation on ... stature, and hearing loss (CATSHL) syndrome. Am J Hum Genet. 2006 Nov;79(5): ...
    https://medlineplus.gov/genetics/gene/fgfr3 - Genetics
  6. Polymicrogyria 
    ... Walsh CA. Bilateral generalized polymicrogyria (BGP): a distinct syndrome of cortical malformation. Neurology. 2004 May 25;62(10):1722-8. doi: 10.1212/01.wnl.0000125187.52952.e9. Citation on PubMed Dobyns WB, Mirzaa G, Christian SL, Petras K, Roseberry J, Clark GD, Curry ...
    https://medlineplus.gov/genetics/condition/polymicrogyria - Genetics
  7. GJA1 gene 
    ... Wollnik B, Keegan CE, Innis JW, Dinulos MB, Christian C, Hannibal MC, Jabs EW. ... in oculodentodigital syndrome/type III syndactyly. J Med Genet. 2004 Jan; ...
    https://medlineplus.gov/genetics/gene/gja1 - Genetics
  8. Oculodentodigital dysplasia 
    ... Stogbauer F. Neurological manifestations of the oculodentodigital dysplasia ... Innis JW, Dinulos MB, Christian C, Hannibal MC, Jabs EW. Connexin 43 (GJA1) ...
    https://medlineplus.gov/.../condition/oculodentodigital-dysplasia - Genetics
  9. Trichothiodystrophy 
    ... deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome ... MC, Introne WJ, Christian T, Verheijen FW, Smith DEC, Mendes MI, Hussaarts- ...
    https://medlineplus.gov/genetics/condition/trichothiodystrophy - Genetics
  10. 16p11.2 deletion syndrome 
    ... TC, Nowak NJ, Cook EH Jr, Dobyns WB, Christian SL. Recurrent 16p11.2 microdeletions in autism. Hum ...
    https://medlineplus.gov/genetics/condition/16p112-deletion-syndrome - Genetics
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