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Volumn 17, Issue 2, 2008, Pages 113-117

The fifth female patient with Myhre syndrome: Further delineation

Author keywords

Blepharophimosis; Cleft palate; Myhre syndrome; Precocious puberty

Indexed keywords

ADOLESCENT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BODY BUILD; BODY MASS; BORDERLINE STATE; CASE REPORT; CLEFT LIP; FACIES; FEMALE; HANDWRITING; HISPANIC; HUMAN; JOINT MOBILITY; MYHRE RUVALCABA SYNDROME; PHENOTYPE; PREMATURE FETUS MEMBRANE RUPTURE; PRIORITY JOURNAL; RADIOLOGY; SHORT STATURE; WECHSLER INTELLIGENCE SCALE;

EID: 41849123119     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/MCD.0b013e3282f52828     Document Type: Article
Times cited : (15)

References (11)
  • 8
    • 41849123762 scopus 로고    scopus 로고
    • OMIM-Online Mendelian Inheritance in Man (2007). McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University (Baltimore, MD) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD), August 7, 2007. World Wide Web URL: http://www.ncbi.nlm.nih.gov/ omim/
    • OMIM-Online Mendelian Inheritance in Man (2007). McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University (Baltimore, MD) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD), August 7, 2007. World Wide Web URL: http://www.ncbi.nlm.nih.gov/ omim/
  • 10
    • 33645851375 scopus 로고    scopus 로고
    • Myhre syndrome in a female with previously undescribed symptoms: Further delineation of the phenotype
    • van Steensel MAM, Vreeburg M, Steijlen PM, de Die-Smulders VC (2005). Myhre syndrome in a female with previously undescribed symptoms: further delineation of the phenotype. Am J Med Genet 139A:127-130.
    • (2005) Am J Med Genet , vol.139 A , pp. 127-130
    • van Steensel, M.A.M.1    Vreeburg, M.2    Steijlen, P.M.3    de Die-Smulders, V.C.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.