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Acta Paediatrica, International Journal of Paediatrics

Volumn 88, Issue 6, 1999, Pages 675-678

Partial trisomy 13q22→qter and monosomy 18q21→qter as a result of familial translocation

(6) Cekada S a Kilvain, S a Brajenovic Milic B b Brecevic L c Kirincic Paucic E a Franulovic J a

a UNIVERSITY OF RIJEKA (Croatia)

b UNIVERSITY OF RIJEKA (Croatia)

c UNIVERSITY OF ZURICH (Switzerland)

Author keywords

FISH; Karyotype; Malformations; Prenatal diagnosis

Indexed keywords

ALPHA FETOPROTEIN;

AMNIOCENTESIS; ARTICLE; CASE REPORT; CHROMOSOME 13Q; CHROMOSOME 18Q; CYTOGENETICS; ELECTROENCEPHALOGRAM; HUMAN; HUMAN CELL; HUMAN TISSUE; KARYOTYPE; MALE; MONOSOMY; NEWBORN; PARTIAL TRISOMY 13; PHENOTYPE; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 18; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; MALE; MONOSOMY; TRANSLOCATION, GENETIC; TRISOMY;

EID: 0033008773 PISSN: 08035253 EISSN: None Source Type: Journal
DOI: 10.1080/08035259950169387 Document Type: Article

Times cited : (6)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.