Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion

Prenatal Diagnosis

Volumn 23, Issue 6, 2003, Pages 504-508

  Chen, Chih Ping ^a,b   Lin, Shuan Pei ^a   Chern, Schu Rern ^a   Shih, Shin Lin ^a   Lee, Chen Chi ^a   Wang, Wayseen ^a   Liao, You Wei ^c  

^a MACKAY MEMORIAL HOSPITAL   (Taiwan)

^b NATIONAL YANG MING UNIVERSITY   (Taiwan)

^c TAIWAN ADVENTIST HOSPITAL   (Taiwan)

Author keywords

22q13 deletion; FISH; Molecular analysis; Trisomy 16q; Ultrasound

Indexed keywords

CEREBROSIDE SULFATASE;

ADULT; APNEA; ARTICLE; CASE REPORT; CHROMOSOME 16Q; CHROMOSOME 22Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME DELETION 22; CLINICAL FEATURE; CLINODACTYLY; DIGEORGE SYNDROME; DNA PROBE; ECHOGRAPHY; EPICANTHUS; FEMALE; FETUS; FETUS MOVEMENT; FLUORESCENCE IN SITU HYBRIDIZATION; FRONTAL BOSSING; GENE LOCUS; GESTATIONAL AGE; HUMAN; HYPERTELORISM; INTRAUTERINE GROWTH RETARDATION; KARYOTYPE 46,XX; MICROGNATHIA; MICROSATELLITE MARKER; MUSCLE HYPOTONIA; PRIORITY JOURNAL; PROMINENT EAR; PTOSIS; SKULL MALFORMATION; TELOMERE; TRISOMY 16; VELOCARDIOFACIAL SYNDROME;

ABNORMALITIES, MULTIPLE; ADULT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 16; CHROMOSOMES, HUMAN, PAIR 22; DNA; FEMALE; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; MALE; PREGNANCY; TRISOMY; ULTRASONOGRAPHY, PRENATAL;

EID: 0037785314     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.629     Document Type: Article

References (10)

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