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Results 1 - 10 of 107 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. Supernumerary nipples 
    ... 2018:chap 64. Bolognia JL, Schaffer JV, Duncan KO, Ko CJ. Developmental anomalies. In: Bolognia JL, Schaffer JV, Duncan KO, Ko CJ, eds. Dermatology Essentials . 2nd ed. Philadelphia, ...
    https://medlineplus.gov/ency/article/003110.htm - Medical Encyclopedia
  4. 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
  5. Keratosis obturans 
    Keratosis obturans (KO) is the buildup of keratin in the ear canal. Keratin is a protein released by skin cells that ... The exact cause of KO is unknown. It may be due to a problem with how skin cells in the ear canal are produced. Or, ...
    https://medlineplus.gov/ency/article/001617.htm - Medical Encyclopedia
  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. 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
  8. 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
  9. 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
  10. 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
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