Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32→qter) and partial monosomy 21q (21q22.2→qter)

Prenatal Diagnosis

Volumn 26, Issue 4, 2006, Pages 313-320

  Chen, Chih Ping ^a,b,c   Chern, Schu Rern ^a   Lin, Chyi Chyang ^d   Wang, Tzu Hao ^e   Li, Yueh Chun ^f   Hsieh, Lie Jiau ^d   Lee, Chen Chi ^a   Hua, Hui Min ^g   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 CHANG GUNG MEMORIAL HOSPITAL   (Taiwan)

^f CHUNG SHAN MEDICAL UNIVERSITY   (Taiwan)

^g YUAN ZE UNIVERSITY   (Taiwan)

Author keywords

21q22.2 deletion; Partial monosomy 21q; Partial trisomy 12q; Prenatal diagnosis; Ultrasound

Indexed keywords

ADULT; AMNIOCENTESIS; CASE REPORT; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION 12; CHROMOSOME TRANSLOCATION 21; DNA POLYMORPHISM; ECHOGRAPHY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETIC MARKER; GESTATION PERIOD; HEART VENTRICLE SEPTUM DEFECT; HOLOPROSENCEPHALY; HUMAN; KARYOTYPING; MEDICAL LITERATURE; MICROCEPHALY; MICROGNATHIA; PARTIAL MONOSOMY; PARTIAL TRISOMY; PHENOTYPE; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; REVIEW;

ADULT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 12; CHROMOSOMES, HUMAN, PAIR 21; CYTOGENETIC ANALYSIS; FEMALE; GENE DELETION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; PREGNANCY; PRENATAL DIAGNOSIS; TRISOMY;

EID: 33646053465     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1399     Document Type: Review

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