Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial duplication of Yq (Yq11.2→qter) and partial monosomy 5p (5p15.3→pter) [5]

Prenatal Diagnosis

Volumn 25, Issue 8, 2005, Pages 723-725

  Chen, Chih Ping ^a,b,c   Lin, Shuan Pei ^a   Lin, Chyi Chyang ^d   Li, Yueh Chun ^e   Hsieh, Lie Jiau ^d   Lee, Chen Chi ^a   Chen, Yen Jiun ^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

[No Author keywords available]

Indexed keywords

ADULT; APGAR SCORE; AUTOSOME; BIOMETRY; CASE REPORT; CHROMOSOME 5; CHROMOSOME DUPLICATION; FEMALE; FETUS DEVELOPMENT; FLUORESCENCE IN SITU HYBRIDIZATION; GESTATIONAL AGE; HUMAN; INTRAUTERINE GROWTH RETARDATION; LETTER; PARTIAL MONOSOMY; PHENOTYPE; PRIORITY JOURNAL; SPECTRAL KARYOTYPING; SRY GENE; Y CHROMOSOME;

ADULT; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 5; CHROMOSOMES, HUMAN, Y; CRI-DU-CHAT SYNDROME; FEMALE; FETAL GROWTH RETARDATION; FLOW CYTOMETRY; FLUORESCENCE; GENE DUPLICATION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; MALE; MONOSOMY; PREGNANCY; ULTRASONOGRAPHY, PRENATAL;

EID: 23844453062     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.1223     Document Type: Letter

References (11)

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