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Volumn 158 A, Issue 7, 2012, Pages 1785-1787

Contribution of LPP copy number and sequence changes to esophageal atresia, tracheoesophageal fistula, and VACTERL association

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ANORECTAL MALFORMATION; ARTICLE; CLINICAL ARTICLE; DISEASE ASSOCIATION; ESOPHAGUS ATRESIA; EXON; GENE; GENE DELETION; GENE DOSAGE; GENE FREQUENCY; GENE FUNCTION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC SCREENING; HEART DISEASE; HOMOZYGOTE; HUMAN; LPP GENE; PHENOTYPE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; TRACHEOESOPHAGEAL FISTULA; VERTEBRA MALFORMATION;

EID: 84862650486     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.35391     Document Type: Article
Times cited : (10)

References (6)
  • 1
    • 78049298308 scopus 로고    scopus 로고
    • Haploinsufficiency of the LIM domain containing preferred translocation partner in lipoma (LPP) gene in patients with tetralogy of Fallot and VACTERL association
    • Arrington CB, Patel A, Bacino CA, Bowles NE. 2010. Haploinsufficiency of the LIM domain containing preferred translocation partner in lipoma (LPP) gene in patients with tetralogy of Fallot and VACTERL association. Am J Med Genet Part A 152A: 2919- 2923.
    • (2010) Am J Med Genet Part A , vol.152 A , pp. 2919-2923
    • Arrington, C.B.1    Patel, A.2    Bacino, C.A.3    Bowles, N.E.4
  • 6
    • 33745906255 scopus 로고    scopus 로고
    • Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology
    • Shaw-Smith CJ. 2006. Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology. J Med Genet 43: 545- 554.
    • (2006) J Med Genet , vol.43 , pp. 545-554
    • Shaw-Smith, C.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.