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Results 1 - 10 of 135 for robert syndrome 3
  1. Lissencephaly with cerebellar hypoplasia 
    ... Lissencephaly 3 Lissencephaly syndrome, Norman-Roberts type Norman-Roberts syndrome Genetic Testing Registry: Lissencephaly type 3 Genetic Testing Registry: Norman-Roberts syndrome Cobblestone lissencephaly ...
    https://medlineplus.gov/.../lissencephaly-with-cerebellar-hypoplasia - Genetics
  2. PRKAG2 gene 
    ... on PubMed Gollob MH, Green MS, Tang AS, Roberts R. PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction system disease, and cardiac hypertrophy. Curr Opin Cardiol. 2002 May;17(3):229-34. doi: 10.1097/00001573-200205000-00004. ...
    https://medlineplus.gov/genetics/gene/prkag2 - Genetics
  3. Noonan syndrome 
    ... Zenker M, Zampino G, Verloes A, Dallapiccola B, Roberts AE, Cave H, Gelb BD, Neel BG, ... Epub 2015 Aug 3. Citation on PubMed or Free article on PubMed ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  4. SOS1 gene 
    ... No abstract available. English, Spanish. Citation on PubMed Roberts ... Dec 3. Citation on PubMed Romano AA, Allanson JE, Dahlgren ...
    https://medlineplus.gov/genetics/gene/sos1 - Genetics
  5. TNXB gene 
    ... TNXB NCBI Gene ClinVar ... syndrome: a cross-sectional study in 17 patients. Clin Genet. 2017 Mar;91(3):411-425. doi: 10.1111/cge.12853. Epub ...
    https://medlineplus.gov/genetics/gene/tnxb - Genetics
  6. Cardiofaciocutaneous syndrome 
    ... Genet A. 2006 Aug 1;140(15):1681-3. doi: 10.1002/ajmg.a.31315. No abstract available. Citation on PubMed Roberts A, Allanson J, Jadico SK, Kavamura MI, Noonan J, Opitz JM, Young T, Neri G. The cardiofaciocutaneous syndrome. J Med Genet. 2006 Nov;43(11):833- ...
    https://medlineplus.gov/.../condition/cardiofaciocutaneous-syndrome - Genetics
  7. 3MC syndrome 
    ... syndrome: variable expression of a single disorder (3MC syndrome)? Am J Med Genet A. 2005 Sep 1;137A(3):332-5. doi: 10.1002/ajmg.a.30878. Citation on PubMed Urquhart J, Roberts R, de Silva D, Shalev S, Chervinsky E, ...
    https://medlineplus.gov/genetics/condition/3mc-syndrome - Genetics
  8. TWNK gene 
    ... twinkle Tests of TWNK PubMed MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE); MTDPS3 TWINKLE mtDNA HELICASE; TWNK NCBI Gene ClinVar Fratter C, Gorman GS, Stewart JD, Buddles M, Smith C, Evans J, Seller A, Poulton J, Roberts M, Hanna MG, Rahman S, Omer SE, Klopstock ...
    https://medlineplus.gov/genetics/gene/twnk - Genetics
  9. TGFBR2 gene 
    ... TGFBR1 or TGFBR2. Nat Genet. 2005 Mar;37(3):275-81. doi: 10.1038/ng1511. Epub ... Dietz HC. Aneurysm syndromes caused by mutations in the TGF-beta receptor. ...
    https://medlineplus.gov/genetics/gene/tgfbr2 - Genetics
  10. CAV3 gene 
    ... VIP-21 VIP21 Tests of CAV3 PubMed CAVEOLIN 3; CAV3 LONG QT SYNDROME 9; LQT9 NCBI Gene ClinVar Aboumousa A, Hoogendijk J, Charlton R, Barresi R, Herrmann R, Voit T, Hudson J, Roberts M, Hilton-Jones D, Eagle M, Bushby K, ...
    https://medlineplus.gov/genetics/gene/cav3 - Genetics
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