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Volumn 43, Issue 12, 2001, Pages 843-846

Deletion of 8p: A report of a child with normal intelligence

Author keywords

[No Author keywords available]

Indexed keywords

ANAMNESIS; ARTICLE; BODY HEIGHT; BODY WEIGHT; CASE REPORT; CHILD DEVELOPMENT; CHILD REARING; CHILDHOOD; CHROMOSOME 8P; CHROMOSOME ANALYSIS; CHROMOSOME ARM; CHROMOSOME DELETION; CHROMOSOME DELETION 8P; CLINICAL FEATURE; COGNITIVE DEVELOPMENT; DISEASE SEVERITY; FEMALE; GROWTH; HUMAN; INTELLECTUAL IMPAIRMENT; INTELLIGENCE; INTELLIGENCE TEST; LANGUAGE ABILITY; LINGUISTICS; MEDICAL LITERATURE; MONITORING; MOTOR RETARDATION; OCCUPATIONAL THERAPY; PHYSIOTHERAPY; PRESCHOOL CHILD; PRIORITY JOURNAL; SOCIAL ADAPTATION; SPEECH THERAPY; WALKING;

EID: 0035207322     PISSN: 00121622     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1469-8749.2001.tb00174.x     Document Type: Article
Times cited : (20)

References (17)
  • 14
    • 0032854607 scopus 로고    scopus 로고
    • A paternally inherited terminal deletion, del(8) (p23.1)pat, detected prenatally in an amniotic fluid sample: A review of deletion 8p23.1 cases
    • (1999) Prenatal Diagnosis , vol.19 , pp. 868-872
    • Reddy, K.S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.