메뉴 건너뛰기




Volumn 58, Issue 4, 1996, Pages 743-748

The locus for a novel syndromic form of neuronal intestinal pseudoobstruction maps to Xq28

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARGENTAFFIN CELL; ARTICLE; CHROMOSOME XQ; CLINICAL ARTICLE; CLINICAL FEATURE; FEMALE; GENE LOCUS; GENETIC LINKAGE; HIRSCHSPRUNG DISEASE; HUMAN; HYPERTROPHIC PYLORUS STENOSIS; INTESTINE INNERVATION; INTESTINE MALROTATION; INTESTINE PSEUDOOBSTRUCTION; MALE; MYENTERIC PLEXUS; PRESCHOOL CHILD; PRIORITY JOURNAL; SHORT BOWEL SYNDROME; X CHROMOSOME LINKED DISORDER;

EID: 0029912523     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (79)

References (5)
  • 3
    • 0029119781 scopus 로고
    • Diversity of the RET proto-oncogene mutations in familial and sporadic Hirschsprung disease
    • Attie' T, Pelet A, Edery P, Eng C, Mulligan LM, Amiel J, Boutrand L, et al (1995a) Diversity of the RET proto-oncogene mutations in familial and sporadic Hirschsprung disease. Hum Mol Genet 4:1381-1386
    • (1995) Hum Mol Genet , vol.4 , pp. 1381-1386
    • Attie, T.1    Pelet, A.2    Edery, P.3    Eng, C.4    Mulligan, L.M.5    Amiel, J.6    Boutrand, L.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.