Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1

Prenatal Diagnosis

Volumn 27, Issue 10, 2007, Pages 967-969

  Chen, Chih Ping ^a,b,c   Wang, Tzu Hao ^d   Chen, Yann Jang ^e,f   Chang, Tung Yao ^a   Liu, Yu Peng ^a   Tzen, Chin Yuan ^a   Chern, Schu Rern ^a   Wang, Wayseen ^a  

^a MACKAY MEMORIAL HOSPITAL   (Taiwan)

^b ASIA UNIVERSITY   (Taiwan)

^c CHINA MEDICAL UNIVERSITY   (Taiwan)

^d CHANG GUNG UNIVERSITY   (Taiwan)

^e NATIONAL YANG MING UNIVERSITY   (Taiwan)

^f TAIPEI VETERANS GENERAL HOSPITAL   (Taiwan)

Author keywords

8p23.1; Fryns syndrome; Microdeletion; MRI; Prenatal diagnosis

Indexed keywords

ADULT; AMNIOTIC FLUID CELL; ARTICLE; CASE REPORT; CEREBELLUM HYPOPLASIA; CHROMOSOME 8P; CHROMOSOME DELETION; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; DELIVERY; DIAPHRAGM HERNIA; ECHOGRAPHY; FEMALE; FRYNS SYNDROME; HEAD CIRCUMFERENCE; HUMAN; HYDRAMNIOS; KARYOTYPE; KIDNEY HYPOPLASIA; LUNG HYPOPLASIA; MACROCEPHALY; MICROGNATHIA; NUCLEAR MAGNETIC RESONANCE IMAGING; PREGNANCY; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIMIGRAVIDA; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; ABORTION, THERAPEUTIC; ADULT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 8; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; PREGNANCY; PREGNANCY TRIMESTER, SECOND; PRENATAL DIAGNOSIS;

EID: 35348956454     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1797     Document Type: Article

References (12)

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