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Results 1 - 10 of 287 for chen syndrome
  1. Lateral meningocele syndrome 
    ... 35968. Epub 2013 May 21. Citation on PubMed Chen CP. Syndromes, disorders and maternal risk factors associated with neural ... S1028-4559(08)60049-2. Citation on PubMed Chen KM, Bird L, Barnes P, Barth R, Hudgins L. Lateral meningocele syndrome: vertical transmission and expansion of the phenotype. Am ...
    https://medlineplus.gov/.../condition/lateral-meningocele-syndrome - Genetics
  2. Donnai-Barrow syndrome 
    ... 10.1002/ajmg.a.20266. Citation on PubMed Chen CP. Syndromes and disorders associated with omphalocele (III): single gene ...
    https://medlineplus.gov/genetics/condition/donnai-barrow-syndrome - Genetics
  3. Grange syndrome 
    ... GRANGE SYNDROME; GRNG PubMed Grange DK, Balfour IC, Chen SC, Wood EG. Familial syndrome of progressive arterial occlusive disease consistent with fibromuscular ...
    https://medlineplus.gov/genetics/condition/grange-syndrome - Genetics
  4. Pfeiffer syndrome 
    ... Organization for Rare Disorders (NORD) ClinicalTrials.gov PFEIFFER SYNDROME PubMed Chen L, Deng CX. Roles of FGF signaling in skeletal development and human genetic diseases. Front Biosci. 2005 May ... and FGFR2 mutations in Pfeiffer syndrome. J Craniofac Surg. 2013 Jan;24(1):150- ...
    https://medlineplus.gov/genetics/condition/pfeiffer-syndrome - Genetics
  5. Androgen insensitivity syndrome 
    ... for Rare Disorders (NORD) ClinicalTrials.gov ANDROGEN INSENSITIVITY SYNDROME; AIS PubMed Chen MJ, Vu BM, Axelrad M, Dietrich JE, Gargollo P, Gunn S, Macias CG, McCullough LB, Roth DR, Sutton VR, Karaviti LP. ... Management Considerations from Infancy to Adulthood. Pediatr Endocrinol ...
    https://medlineplus.gov/.../androgen-insensitivity-syndrome - Genetics
  6. Beare-Stevenson cutis gyrata syndrome 
    ... for Rare Disorders (NORD) BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS PubMed Chen L, Deng CX. Roles of FGF signaling in skeletal development and human genetic diseases. Front Biosci. 2005 May ... of Beare-Stevenson syndrome with a Tyr375Cys mutation in the fibroblast growth ...
    https://medlineplus.gov/.../beare-stevenson-cutis-gyrata-syndrome - Genetics
  7. Polycystic ovary syndrome 
    ... on PubMed Zhao H, Lv Y, Li L, Chen ZJ. Genetic Studies on Polycystic Ovary Syndrome. Best Pract Res Clin Obstet Gynaecol. 2016 Nov; ...
    https://medlineplus.gov/genetics/condition/polycystic-ovary-syndrome - Genetics
  8. Ataxia-pancytopenia syndrome 
    ... PANCYTOPENIA SYNDROME; ATXPC MONOSOMY 7 MYELODYSPLASIA AND LEUKEMIA SYNDROME 1; M7MLS1 PubMed Chen DH, Below JE, Shimamura A, Keel SB, Matsushita M, Wolff J, Sul Y, Bonkowski E, Castella M, Taniguchi T, Nickerson D, Papayannopoulou T, Bird ... Syndrome Is Caused by Missense Mutations in SAMD9L. Am ...
    https://medlineplus.gov/.../condition/ataxia-pancytopenia-syndrome - Genetics
  9. Noonan syndrome 
    ... SYNDROME 6; NS6 NOONAN SYNDROME 9; NS9 NOONAN SYNDROME 10; NS10 PubMed Chen PC, Yin J, Yu HW, Yuan T, Fernandez M, Yung CK, Trinh QM, Peltekova VD, Reid JG, Tworog-Dube E, Morgan MB, Muzny ... variants associated with Noonan syndrome. Proc Natl Acad Sci U S A. 2014 ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  10. Felty syndrome 
    ... nlm.nih.gov/29217783/ . Wang CR, Chiu YC, Chen YC. Successful treatment of refractory neutropenia in Felty's syndrome with rituximab. Scand J Rheumatol . 2018;47(4): ...
    https://medlineplus.gov/ency/article/000445.htm - Medical Encyclopedia
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