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Results 1 - 10 of 200 for cm
  1. CHD7 gene 
    ... A, Bocca G, Hoefsloot LH, van Ravenswaaij-Arts CM. The results of CHD7 analysis in clinically well- ... LH, Jongmans MC, Hofstra RM, van Ravenswaaij-Arts CM. CHD7 mutations and CHARGE syndrome: the clinical implications ...
    https://medlineplus.gov/genetics/gene/chd7 - Genetics
  2. TG gene 
    ... Free article on PubMed Central Caron P, Moya CM, Malet D, Gutnisky VJ, Chabardes B, Rivolta CM, Targovnik HM. Compound heterozygous mutations in the thyroglobulin ...
    https://medlineplus.gov/genetics/gene/tg - Genetics
  3. RASA1 gene 
    ... found to cause capillary malformation-arteriovenous malformation syndrome (CM-AVM), which is a condition characterized by abnormalities ... vascular system. Most of the mutations responsible for CM-AVM prevent the production of functional p120-RasGAP ...
    https://medlineplus.gov/genetics/gene/rasa1 - Genetics
  4. TIMM8A gene 
    ... ND, Lodahl M, Ng K, Rowe DB, Sue CM, Hayes MW, Tranebjaerg L, Fung VS. The phenotypic ... PubMed Roesch K, Curran SP, Tranebjaerg L, Koehler CM. Human deafness dystonia syndrome is caused by a ...
    https://medlineplus.gov/genetics/gene/timm8a - Genetics
  5. BRAF gene 
    ... nih.gov/books/NBK1383/ Citation on PubMed Harmon CM, Brown N. Langerhans Cell Histiocytosis: A Clinicopathologic Review ... B, Pierpont ME, Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features, diagnosis, and ...
    https://medlineplus.gov/genetics/gene/braf - Genetics
  6. PHOX2B gene 
    ... Gene ClinVar Berry-Kravis EM, Zhou L, Rand CM, Weese-Mayer DE. Congenital central hypoventilation syndrome: PHOX2B ... Abara SG, Zhou L, Berry-Kravis EM, Rand CM, Weese-Mayer DE. Later-onset congenital central hypoventilation ...
    https://medlineplus.gov/genetics/gene/phox2b - Genetics
  7. SCNN1B gene 
    ... Epub 2011 Sep 29. Citation on PubMed Canessa CM, Schild L, Buell G, Thorens B, Gautschi I, ... Citation on PubMed Shimkets RA, Warnock DG, Bositis CM, Nelson-Williams C, Hansson JH, Schambelan M, Gill ...
    https://medlineplus.gov/genetics/gene/scnn1b - Genetics
  8. IL23R gene 
    ... ER, Satsangi J, Fisher SA, Forbes A, Lewis CM, Onnie CM, Prescott NJ, Sanderson J, Matthew CG, Barbour J, ... GA, Walker M, Elliott KS, Groves CJ, Lindgren CM, Rayner NW, Timpson NJ, Zeggini E, Newport M, ...
    https://medlineplus.gov/genetics/gene/il23r - Genetics
  9. MMAB gene 
    ... PubMed or Free article on PubMed Central Dobson CM, Wai T, Leclerc D, Kadir H, Narang M, ... AB, Watkins D, Tirone JC, Villeneuve A, Dobson CM, Montpetit A, Lepage P, Gravel RA, Rosenblatt DS. ...
    https://medlineplus.gov/genetics/gene/mmab - Genetics
  10. KRAS gene 
    ... B, Pierpont ME, Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features, diagnosis, and ... N, Nguyen H, Kratz CP, Zenker M, Niemeyer CM, Molven A, Shannon K. Biochemical and functional characterization ...
    https://medlineplus.gov/genetics/gene/kras - Genetics
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