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Annales de Genetique

Volumn 45, Issue 2, 2002, Pages 53-57

Trisomy 4q syndrome: Presentation of a new case and review of the literature

(5) Lundin, Catarina a Zech, Lore a Sjörs, Kerstin b Wadelius, Claes a Annerén, Göran a,c

a UPPSALA UNIVERSITY (Sweden)

b CENTRAL HOSPITAL (Sweden)

c UNIVERSITY CHILDREN S HOSPITAL (Sweden)

Author keywords

De novo partial trisomy; Mental retardation; Trisomy 4q syndrome

Indexed keywords

DNA;

ADOLESCENT; ARTICLE; CASE REPORT; CHROMOSOME 4; CLINICAL FEATURE; CYTOGENETICS; DNA DETERMINATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENOTYPE; HUMAN; KARYOTYPE; MENTAL DEFICIENCY; PHENOTYPE; TRISOMY; TRISOMY 4Q SYNDROME; CHROMOSOME ANALYSIS; GENE TRANSLOCATION; GENETICS; GROWTH DISORDER; HEARING LOSS; NUCLEOTIDE SEQUENCE; REVIEW; SYNDROME;

ADOLESCENT; CASE REPORT; CHROMOSOMES, HUMAN, PAIR 4; CYTOGENETIC ANALYSIS; DNA MUTATIONAL ANALYSIS; FEMALE; GROWTH DISORDERS; HEARING LOSS; HUMAN; IN SITU HYBRIDIZATION, FLUORESCENCE; MENTAL RETARDATION; SUPPORT, NON-U.S. GOV'T; SYNDROME; TRANSLOCATION (GENETICS); TRISOMY; HUMANS; TRANSLOCATION, GENETIC;

EID: 0036021289 PISSN: 00033995 EISSN: None Source Type: Journal
DOI: 10.1016/S0003-3995(02)01117-6 Document Type: Article

Times cited : (35)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.