Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3→q31.3) associated with Gorlin syndrome

Prenatal Diagnosis

Volumn 26, Issue 8, 2006, Pages 725-729

  Chen, Chih Ping ^a,b,c   Lin, Shuan Pei ^a   Wang, Tzu Hao ^d   Chen, Yann Jang ^b,e   Chen, Ming ^f   Wang, Wayseen ^a  

^a MACKAY MEMORIAL HOSPITAL   (Taiwan)

^b NATIONAL YANG MING UNIVERSITY   (Taiwan)

^c CHINA MEDICAL UNIVERSITY   (Taiwan)

^d CHANG GUNG UNIVERSITY   (Taiwan)

^e TAIPEI VETERANS GENERAL HOSPITAL   (Taiwan)

^f CHANGHUA CHRISTIAN HOSPITAL   (Taiwan)

Author keywords

Array comparative genomic hybridization (CGH); Fluorescence in situ hybridization (FISH); Gorlin syndrome; Interstitial deletion of 9q; Maternal serum screening; PTCH gene

Indexed keywords

ALPHA FETOPROTEIN; CHORIONIC GONADOTROPIN; DNA MARKER; PROTEIN PATCHED;

ADULT; AMNIOCENTESIS; ARTICLE; BASAL CELL NEVUS SYNDROME; CASE REPORT; CHROMOSOME 9Q; CHROMOSOME ANALYSIS; CHROMOSOME BANDING PATTERN; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; DOWN SYNDROME; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GESTATION PERIOD; HOSPITAL; HUMAN; KARYOTYPE 46,XY; MACROCEPHALY; MATERNAL SERUM; MOLECULAR GENETICS; NORMAL HUMAN; PERIPHERAL LYMPHOCYTE; PRIMIGRAVIDA; PRIORITY JOURNAL; RISK ASSESSMENT;

ADULT; ALPHA-FETOPROTEINS; AMNIOCENTESIS; BASAL CELL NEVUS SYNDROME; CHORIONIC GONADOTROPIN; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; MALE; PREGNANCY; RECEPTORS, CELL SURFACE;

EID: 33747410543     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1496     Document Type: Article

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