Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 21 - 30 of 675 for p phenotype
  1. BSCL2 gene 
    ... Visser BW, Meggouh F, Weterman MA, De Jonghe P, Timmerman V, de Visser M. Phenotype of Charcot-Marie-Tooth disease Type 2. Neurology. ...
    https://medlineplus.gov/genetics/gene/bscl2 - Genetics
  2. Pantothenate kinase-associated neurodegeneration 
    ... Marelli C, Di Giorgio A, Coubes P, Barone P, Dallapiccola B. The diverse phenotype and genotype of pantothenate kinase-associated neurodegeneration. Neurology. ...
    https://medlineplus.gov/...enate-kinase-associated-neurodegeneration - Genetics
  3. TECTA gene 
    ... P, Devoto M, Zenner HP, Blin N, Nurnberg P, Ozkarakas H, Kupka S. A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations. Cell Physiol Biochem. 2004;14(4-6):369-76. doi: ... Schatteman I, Verstreken M, Van Hauwe P, Coucke P, Chen A, Smith RJ, Somers T, ...
    https://medlineplus.gov/genetics/gene/tecta - Genetics
  4. AMELX gene 
    ... K, Seow K, Crawford P, Aldred MJ, Hart PS, Hart TC. Amelogenesis imperfecta: genotype-phenotype studies in 71 families. Cells Tissues Organs. 2011; ...
    https://medlineplus.gov/genetics/gene/amelx - Genetics
  5. Amelogenesis imperfecta 
    ... K, Seow K, Crawford P, Aldred MJ, Hart PS, Hart TC. Amelogenesis imperfecta: genotype-phenotype studies in 71 families. Cells Tissues Organs. 2011; ...
    https://medlineplus.gov/genetics/condition/amelogenesis-imperfecta - Genetics
  6. Cleidocranial dysplasia 
    ... PubMed Jaruga A, Hordyjewska E, Kandzierski G, Tylzanowski P. Cleidocranial dysplasia and RUNX2-clinical phenotype-genotype correlation. Clin Genet. 2016 Nov;90(5): ...
    https://medlineplus.gov/genetics/condition/cleidocranial-dysplasia - Genetics
  7. RUNX2 gene 
    ... PubMed Jaruga A, Hordyjewska E, Kandzierski G, Tylzanowski P. Cleidocranial dysplasia and RUNX2-clinical phenotype-genotype correlation. Clin Genet. 2016 Nov;90(5): ...
    https://medlineplus.gov/genetics/gene/runx2 - Genetics
  8. Congenital nephrotic syndrome 
    ... O, Pawtowski A, Brandstrom P, Loirat C, Niaudet P, Gubler MC, Antignac C. Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome. J ...
    https://medlineplus.gov/.../condition/congenital-nephrotic-syndrome - Genetics
  9. Campomelic dysplasia 
    ... PubMed Mansour S, Offiah AC, McDowall S, Sim P, Tolmie J, Hall C. The phenotype of survivors of campomelic dysplasia. J Med Genet. ...
    https://medlineplus.gov/genetics/condition/campomelic-dysplasia - Genetics
  10. NPHS2 gene 
    ... O, Pawtowski A, Brandstrom P, Loirat C, Niaudet P, Gubler MC, Antignac C. Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome. J ...
    https://medlineplus.gov/genetics/gene/nphs2 - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next