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Results 1 - 7 of 7 for orth
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  1. Microphthalmia with linear skin defects syndrome 
    ... Wimplinger I, Morleo M, Rosenberger G, Iaconis D, Orth U, Meinecke P, Lerer I, Ballabio A, Gal ... article on PubMed Central Wimplinger I, Rauch A, Orth U, Schwarzer U, Trautmann U, Kutsche K. Mother ...
    https://medlineplus.gov/...thalmia-with-linear-skin-defects-syndrome - Genetics
  2. Autosomal dominant congenital stationary night blindness 
    ... STATIONARY, AUTOSOMAL DOMINANT 1; CSNBAD1 PubMed Gal A, Orth U, Baehr W, Schwinger E, Rosenberg T. Heterozygous ...
    https://medlineplus.gov/...ant-congenital-stationary-night-blindness - Genetics
  3. X chromosome 
    ... article on PubMed Central Wimplinger I, Rauch A, Orth U, Schwarzer U, Trautmann U, Kutsche K. Mother ...
    https://medlineplus.gov/genetics/chromosome/x - Genetics
  4. Potassium-aggravated myotonia 
    ... Apr 29. Citation on PubMed Lehmann-Horn F, Orth M, Kuhn M, Jurkat-Rott K. A novel ...
    https://medlineplus.gov/.../condition/potassium-aggravated-myotonia - Genetics
  5. PDE6B gene 
    ... PHOSPHODIESTERASE 6B; PDE6B NCBI Gene ClinVar Gal A, Orth U, Baehr W, Schwinger E, Rosenberg T. Heterozygous ...
    https://medlineplus.gov/genetics/gene/pde6b - Genetics
  6. SP110 gene 
    ... Bloch DB, Nakajima A, Gulick T, Chiche JD, Orth D, de La Monte SM, Bloch KD. Sp110 ...
    https://medlineplus.gov/genetics/gene/sp110 - Genetics
  7. HCCS gene 
    ... Wimplinger I, Morleo M, Rosenberger G, Iaconis D, Orth U, Meinecke P, Lerer I, Ballabio A, Gal ...
    https://medlineplus.gov/genetics/gene/hccs - Genetics