Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2→q11.21)

Taiwanese Journal of Obstetrics and Gynecology

Volumn 52, Issue 1, 2013, Pages 147-151

  Chen, Chih Ping ^a,b,c,d,e   Ko, Tsang Ming ^f   Su, Yi Ning ^g   Su, Jun Wei ^b,h   Chen, Yu Ting ^b   Lee, Chen Chi ^b   Chen, Li Feng ^b   Wang, Wayseen ^b,i  

^a MACKAY MEDICAL COLLEGE   (Taiwan)

^b MACKAY MEMORIAL HOSPITAL   (Taiwan)

^c ASIA UNIVERSITY   (Taiwan)

^d CHINA MEDICAL UNIVERSITY   (Taiwan)

^e NATIONAL YANG MING UNIVERSITY   (Taiwan)

^f Genephile Bioscience Laboratory   (Taiwan)

^g TAIPEI MEDICAL UNIVERSITY   (Taiwan)

^h CHINA MEDICAL UNIVERSITY HOSPITAL   (Taiwan)

ⁱ TATUNG UNIVERSITY   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AMNIOCENTESIS; AMNION CELL; ARTICLE; BLOOD SAMPLING; CASE REPORT; CHROMOSOME DELETION 22Q11; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; DIGEORGE SYNDROME; FEMALE; GENE LOCUS; GESTATIONAL AGE; HAPLOINSUFFICIENCY; HUMAN; KARYOTYPE; MICROCHIP ANALYSIS; MOLECULAR BIOLOGY; MOLECULAR PROBE; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; PREGNANCY; PRENATAL DIAGNOSIS; UMBILICAL CORD BLOOD;

AMNIOCENTESIS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; GENETIC TESTING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; MULTIPLEX POLYMERASE CHAIN REACTION; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 84878015629     PISSN: 10284559     EISSN: 18756263     Source Type: Journal    
DOI: 10.1016/j.tjog.2012.09.037     Document Type: Article

References (19)

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