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Volumn 10, Issue 3, 1999, Pages 325-327

Familial deletion of 22q11.2

Author keywords

Deletion of 22q.11.2; Schizophrenia; Tetralogy of Fallot; Velo cardio facial syndrome

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 22Q; CHROMOSOME DELETION; DEVELOPMENTAL DISORDER; FACIES; FALLOT TETRALOGY; FEMALE; HUMAN; INFANT; INTELLIGENCE QUOTIENT; MALE; PSYCHOMOTOR DISORDER; SCHIZOPHRENIA; VOICE;

EID: 0032881041     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (2)

References (10)
  • 2
    • 0028895193 scopus 로고
    • Family studies in chromosome 22q11 deletion : Further demonstration of phenotypic heterogeneity
    • DE SILVA D., DUFFTY P., BOOTH P., AUCHTERLONIE I., MORRISON N., DEAN J. C. S.: Family studies in chromosome 22q11 deletion : further demonstration of phenotypic heterogeneity. Clin. Dysmorph., 1995, 4, 294-303
    • (1995) Clin. Dysmorph. , vol.4 , pp. 294-303
    • De Silva, D.1    Duffty, P.2    Booth, P.3    Auchterlonie, I.4    Morrison, N.5    J C S, D.6
  • 3
    • 0000399572 scopus 로고
    • Congenital absence of the thymus and its immunologic consequences: Concurrence with congenital hypoparathyroidism
    • DIGEORGE A. M.: Congenital absence of the thymus and its immunologic consequences: concurrence with congenital hypoparathyroidism. Birth Defects Orig. Art. Ser., 1968, IV(1), 116-121.
    • (1968) Birth Defects Orig. Art. Ser. , vol.4 , Issue.1 , pp. 116-121
    • DiGeorge, A.M.1
  • 6
    • 0014384341 scopus 로고
    • Familial syndrome of right-sided aortic arch, mental deficiency, and facial dysmorphysm
    • STRONG W. B.: Familial syndrome of right-sided aortic arch, mental deficiency, and facial dysmorphysm. J. Pediatr., 1968, 73, 882-888.
    • (1968) J. Pediatr. , vol.73 , pp. 882-888
    • Strong, W.B.1
  • 7
    • 0019352243 scopus 로고
    • The velo-cardio-facial syndrome: A clinical and genetic analysis
    • SHPRINTZEN R. J., GOLDBERG R.B., YOUNG D., WOLFORD L.: The velo-cardio-facial syndrome: a clinical and genetic analysis. Pediatrics, 1981, 67, 167-172.
    • (1981) Pediatrics , vol.67 , pp. 167-172
    • Shprintzen, R.J.1    Goldberg, R.B.2    Young, D.3    Wolford, L.4
  • 9
    • 0002055560 scopus 로고
    • Etiologic categorization of common congenital heart disease
    • Van Praagh R., Takao A. (eds). Mount Kisco N. Y.: Futura Publishing Company (pub.)
    • TAKAO A., ANDO M., CHO K., KINOUCHI A., MURAKAMI Y.: Etiologic categorization of common congenital heart disease. In: Etiology and Morphogenesis of Congenital Heart Disease. Van Praagh R., Takao A. (eds). Mount Kisco N. Y.: Futura Publishing Company (pub.), 1980, 253-269.
    • (1980) Etiology and Morphogenesis of Congenital Heart Disease , pp. 253-269
    • Takao, A.1    Ando, M.2    Cho, K.3    Kinouchi, A.4    Murakami, Y.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.