Wiedemann-Bekwith syndrome: Further prenatal characterization of the condition

American Journal of Medical Genetics

Volumn 107, Issue 3, 2002, Pages 209-213

  Dolfin, Tzipora ^a   Herman, Arie ^a   Heyman, Eli ^a   Amiel, Aliza ^a   Reish, Orit ^a  

^a Genetic Institute   (Israel)

Author keywords

11p15.5 duplication; Prenatal diagnosis; Uniparental disomy

Indexed keywords

ARTICLE; BECKWITH WIEDEMANN SYNDROME; CASE REPORT; CHROMOSOME 11P; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME TRANSLOCATION 11; EARLY DIAGNOSIS; FETUS; FETUS MALFORMATION; GENE AMPLIFICATION; GENE LOCUS; GENE MAPPING; HUMAN; HYDRAMNIOS; INFANT; KARYOTYPE; PARTIAL TRISOMY; PATIENT COUNSELING; PERINATAL PERIOD; PLACENTA DISORDER; POLYMERASE CHAIN REACTION; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SYNDROME DELINEATION; UNIPARENTAL DISOMY; ADULT; CHROMOSOME 11; CHROMOSOME 6; ECHOGRAPHY; FAMILY HEALTH; FATALITY; FEMALE; FETUS DISEASE; GENE TRANSLOCATION; GENETICS; KARYOTYPING; MALE; NEWBORN; PEDIGREE; PREGNANCY; REVIEW;

ADULT; BECKWITH-WIEDEMANN SYNDROME; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 6; FAMILY HEALTH; FATAL OUTCOME; FEMALE; FETAL DISEASES; HUMANS; INFANT, NEWBORN; KARYOTYPING; MALE; PEDIGREE; PREGNANCY; TRANSLOCATION, GENETIC; ULTRASONOGRAPHY, PRENATAL; UNIPARENTAL DISOMY;

EID: 0037154001     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10143     Document Type: Article

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