Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements

Prenatal Diagnosis

Volumn 26, Issue 2, 2006, Pages 138-146

  Chen, Chih Ping ^a,b,c   Chern, Schu Rern ^a   Lee, Chen Chi ^a   Lin, Chyi Chyang ^d   Li, Yueh Chun ^e   Hsieh, Lie Jiau ^d   Chen, Wen Lin ^a   Wang, Wayseen ^a  

^a MACKAY MEMORIAL HOSPITAL   (Taiwan)

^b NATIONAL YANG MING UNIVERSITY   (Taiwan)

^c CHINA MEDICAL UNIVERSITY   (Taiwan)

^d CHINA MEDICAL UNIVERSITY HOSPITAL   (Taiwan)

^e CHUNG SHAN MEDICAL UNIVERSITY   (Taiwan)

Author keywords

Chromosome 10q deletion; Chromosome 5q duplication; Chromosome 7p deletion; Complex chromosomal rearrangement (CCR); De novo; Prenatal diagnosis

Indexed keywords

ALPHA FETOPROTEIN; CHORIONIC GONADOTROPIN;

ADULT; AMNIOCENTESIS; ARTICLE; CASE REPORT; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME TRANSLOCATION 14; CHROMOSOME TRANSLOCATION 18; CHROMOSOME TRANSLOCATION 2; CLINICAL FEATURE; CLINODACTYLY; DNA POLYMORPHISM; DOWN SYNDROME; FACE DYSMORPHIA; FEMALE; GESTATIONAL AGE; HUMAN; HYPOPLASIA; KARYOTYPE 46,XY; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RISK FACTOR; SPECTRAL KARYOTYPING;

ABNORMALITIES, MULTIPLE; ADULT; AMNIOCENTESIS; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 14; CHROMOSOMES, HUMAN, PAIR 18; CHROMOSOMES, HUMAN, PAIR 2; FEMALE; FETAL DISEASES; GENE DUPLICATION; HUMANS; KARYOTYPING; PREGNANCY; PRENATAL DIAGNOSIS; TRANSLOCATION, GENETIC;

EID: 33344456106     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.1369     Document Type: Article

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