메뉴 건너뛰기




Volumn 129 A, Issue 1, 2004, Pages 95-97

Is brachydactyly type ballard a variant of brachydactyly type E? [2]

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ALBRIGHT SYNDROME; BALLARD SYNDROME; BRACHYDACTYLY; CASE REPORT; DISEASE CLASSIFICATION; FAMILY HISTORY; FEMALE; HAND RADIOGRAPHY; HUMAN; HYPOPLASIA; LETTER; MALE; METACARPAL BONE; METATARSAL BONE; PHALANX; PRIORITY JOURNAL; THUMB MALFORMATION; TURNER SYNDROME;

EID: 3342996668     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter
Times cited : (2)

References (12)
  • 1
    • 0025922703 scopus 로고
    • G protein Gs-alpha (GNAS1), the probable candidate gene for Albright hereditary osteodystrophy, is assigned to human chromosome 20q12-q13.2
    • Gopal Rao VVN, Schnittger S, Hansmann I. 1991. G protein Gs-alpha (GNAS1), the probable candidate gene for Albright hereditary osteodystrophy, is assigned to human chromosome 20q12-q13.2. Genomics 10:257-261.
    • (1991) Genomics , vol.10 , pp. 257-261
    • Gopal Rao, V.V.N.1    Schnittger, S.2    Hansmann, I.3
  • 2
    • 0014307514 scopus 로고
    • Brachydactyly and pseudo-pseudohypoparathyroidism
    • Hertzog KP. 1968. Brachydactyly and pseudo-pseudohypoparathyroidism. Acta Genet Med Gemellol 17:428-437.
    • (1968) Acta Genet Med Gemellol , vol.17 , pp. 428-437
    • Hertzog, K.P.1
  • 3
    • 33646215618 scopus 로고    scopus 로고
    • Deletion of GPR35 gene on 2q37.3 may account for Albright hereditary osteodystrophy like phenotype: Defining further genetic variants within and around GPR35 gene
    • Hoo JJ, Shrimpton AE, Braddock BR, Thomson LL, Stein CS. 2003. Deletion of GPR35 gene on 2q37.3 may account for Albright hereditary osteodystrophy like phenotype: Defining further genetic variants within and around GPR35 gene. Am J Hum Genet 73:A653.
    • (2003) Am J Hum Genet , vol.73
    • Hoo, J.J.1    Shrimpton, A.E.2    Braddock, B.R.3    Thomson, L.L.4    Stein, C.S.5
  • 8
    • 0021854061 scopus 로고
    • A new brachydactyly syndrome with similarities to Julia Bell types B and E
    • Pitt P, Williams I. 1985. A new brachydactyly syndrome with similarities to Julia Bell types B and E. J Med Genet 22:202-204.
    • (1985) J Med Genet , vol.22 , pp. 202-204
    • Pitt, P.1    Williams, I.2
  • 9
    • 0030916590 scopus 로고    scopus 로고
    • RDCI, the vasoactive intestinal peptide receptor: A candidate gene for the features of Albright hereditary osteodystrophy associated with deletion 2q37
    • Power MM, James RS, Barber JCK, Fisher AM, Wood PJ, Leatherdale BA, Flanagan DEH, Hatchwell E. 1997. RDCI, the vasoactive intestinal peptide receptor: A candidate gene for the features of Albright hereditary osteodystrophy associated with deletion 2q37. J Med Genet 34:287-290.
    • (1997) J Med Genet , vol.34 , pp. 287-290
    • Power, M.M.1    James, R.S.2    Barber, J.C.K.3    Fisher, A.M.4    Wood, P.J.5    Leatherdale, B.A.6    Flanagan, D.E.H.7    Hatchwell, E.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.