Prenatal diagnosis of de novo isochromosome 13q associated with microcephaly, alobar holoprosencephaly and cebocephaly in a fetus

Prenatal Diagnosis

Volumn 18, Issue 4, 1998, Pages 393-398

  Chen, Chih Ping ^a   Chern, Schu Rern ^a   Lee, Chen Chi ^a   Chen, Li Feng ^a   Chuang, Chun Yu ^a   Chen, Ming Hong ^a  

^a MACKAY MEMORIAL HOSPITAL   (Taiwan)

Author keywords

Cebocephaly; FISH; Holoprosencephaly; Isochromosome 13q; Polymorphic molecular analysis; Prenatal diagnosis

Indexed keywords

ADULT; AMNIOCENTESIS; ARTICLE; AUTOPSY; CASE REPORT; CEBOCEPHALY; CHROMOSOME 13Q; CHROMOSOME ANALYSIS; CORDOCENTESIS; CRANIOFACIAL MALFORMATION; FEMALE; FETUS; FETUS ECHOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ANALYSIS; GENETIC COUNSELING; HEART VENTRICLE SEPTUM DEFECT; HOLOPROSENCEPHALY; HUMAN; HYPOTELORISM; INTRAUTERINE GROWTH RETARDATION; ISOCHROMOSOME; MICROCEPHALY; PATHOLOGY; POLYDACTYLY; PRENATAL DIAGNOSIS; PRIMIGRAVIDA; PRIORITY JOURNAL; TRISOMY 13;

ADULT; AMNIOCENTESIS; CHROMOSOMES, HUMAN, PAIR 13; CRANIOFACIAL ABNORMALITIES; FEMALE; GESTATIONAL AGE; HOLOPROSENCEPHALY; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; ISOCHROMOSOMES; KARYOTYPING; MICROCEPHALY; PREGNANCY; ULTRASONOGRAPHY, PRENATAL;

EID: 0031968466     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199804)18:4<393::AID-PD277>3.0.CO;2-Q     Document Type: Article

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