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American Journal of Medical Genetics

Volumn 98, Issue 1, 2001, Pages 103-106

Mother to son transmission of del(1)(q42.1q42.3)

(4) Sanford Hanna, Julie A a Ball, Susie b Pagon, Roberta A c Donlan, Michael d

a SACRED HEART MEDICAL CENTER (United States)

b Children's Village and Yakima Valley Memorial Hospital (United States)

c SEATTLE CHILDREN S RESEARCH INSTITUTE (United States)

d Inland Northwest Genetics Clinic (United States)

Author keywords

Chromosome 1; Chromosome deletion; Familial chromosome deletion

Indexed keywords

ADULT; ARTICLE; AUTOSOME; CASE REPORT; CHROMOSOME 1Q; CHROMOSOME ANALYSIS; CHROMOSOME ARM; CLINICAL FEATURE; EXTRACHROMOSOMAL INHERITANCE; FEMALE; GENETIC SCREENING; HUMAN; INTERSTITIAL CHROMOSOME DELETION; MALE; PATHOGENESIS; POINT MUTATION; PRIORITY JOURNAL; SCHOOL CHILD;

ABNORMALITIES, MULTIPLE; ADULT; BEHAVIORAL SYMPTOMS; CHILD; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 1; CRANIOFACIAL ABNORMALITIES; CYTOGENETIC ANALYSIS; DISEASE TRANSMISSION, VERTICAL; FAMILY HEALTH; FEMALE; HUMANS; MALE; MOTHERS; PHENOTYPE;

EID: 0035153520 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/1096-8628(20010101)98:1<103::AID-AJMG1005>3.0.CO;2-N Document Type: Article

Times cited : (6)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.