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 1 - 10 of 61 for ko
  1. Kaufman oculocerebrofacial syndrome 
    ... the condition. Blepharophimosis-ptosis-intellectual disability syndrome BPIDS KOS Oculocerebrofacial syndrome, Kaufman type Genetic Testing Registry: Oculocerebrofacial ...
    https://medlineplus.gov/.../kaufman-oculocerebrofacial-syndrome - Genetics
  2. UBE3B gene 
    ... Health Condition BPIDS HECT-type ubiquitin transferase E3B KOS ubiquitin-protein ligase E3B isoform 1 ubiquitin-protein ...
    https://medlineplus.gov/genetics/gene/ube3b - Genetics
  3. COL4A5 gene 
    ... 5; COL4A5 NCBI Gene ClinVar Gross O, Netzer KO, Lambrecht R, Seibold S, Weber M. Meta-analysis ... G, Renieri A, Weber M, Gross O, Netzer KO, Flinter F, Pirson Y, Dahan K, Wieslander J, ...
    https://medlineplus.gov/genetics/gene/col4a5 - Genetics
  4. MCCC1 gene 
    ... S, Moslinger D, Pasquini E, Santer R, Schwab KO, Wilcken B, Fowler B, Yue WW, Baumgartner MR. ... JM, Ranieri E, Das AM, Spiekerkotter U, Schwab KO, Potzsch S, Marquardt I, Hennermann JB, Knerr I, ...
    https://medlineplus.gov/genetics/gene/mccc1 - Genetics
  5. MCCC2 gene 
    ... S, Moslinger D, Pasquini E, Santer R, Schwab KO, Wilcken B, Fowler B, Yue WW, Baumgartner MR. ... JM, Ranieri E, Das AM, Spiekerkotter U, Schwab KO, Potzsch S, Marquardt I, Hennermann JB, Knerr I, ...
    https://medlineplus.gov/genetics/gene/mccc2 - Genetics
  6. Roberts syndrome 
    ... E, Hurst JA, Forzano F, Meins M, Simola KO, Raas-Rothschild A, Schultz RA, McDaniel LD, Ozono ... E, Hurst JA, Forzano F, Meins M, Simola KO, Raas-Rothschild A, Hennekam RC, Jabs EW. Phenotypic ...
    https://medlineplus.gov/genetics/condition/roberts-syndrome - Genetics
  7. ESCO2 gene 
    ... E, Hurst JA, Forzano F, Meins M, Simola KO, Raas-Rothschild A, Schultz RA, McDaniel LD, Ozono ... E, Hurst JA, Forzano F, Meins M, Simola KO, Raas-Rothschild A, Hennekam RC, Jabs EW. Phenotypic ...
    https://medlineplus.gov/genetics/gene/esco2 - Genetics
  8. Alport syndrome 
    ... G, Renieri A, Weber M, Gross O, Netzer KO, Flinter F, Pirson Y, Dahan K, Wieslander J, ... G, Renieri A, Weber M, Gross O, Netzer KO, Flinter F, Pirson Y, Verellen C, Wieslander J, ...
    https://medlineplus.gov/genetics/condition/alport-syndrome - Genetics
  9. 3-methylcrotonyl-CoA carboxylase deficiency 
    ... S, Moslinger D, Pasquini E, Santer R, Schwab KO, Wilcken B, Fowler B, Yue WW, Baumgartner MR. ... JM, Ranieri E, Das AM, Spiekerkotter U, Schwab KO, Potzsch S, Marquardt I, Hennermann JB, Knerr I, ...
    https://medlineplus.gov/...methylcrotonyl-coa-carboxylase-deficiency - Genetics
  10. Distal 18q deletion syndrome 
    ... TH, Pihko SH, Somer MS, Tienari PJ, Wirtavuori KO, Valanne LK. 18q-syndrome: brain MRI shows poor ...
    https://medlineplus.gov/.../condition/distal-18q-deletion-syndrome - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · next