Recurrent trisomy 21 and uniparental disomy 21 in a family

Fetal Diagnosis and Therapy

Volumn 18, Issue 6, 2003, Pages 454-458

  Bán, Zoltán ^a   Nagy, Bálint ^a   Papp, Csaba ^a   Beke, Artúr ^a   Tóth Pál, Erno ^a   Papp, Zoltán ^a  

^a SEMMELWEIS UNIVERSITY   (Hungary)

Author keywords

Down syndrome; Fluorescent PCR; Risk, aneuploidy; Trisomy 21; Uniparental disomy

Indexed keywords

DNA;

ADULT; AMNION FLUID ANALYSIS; AMNION FLUID CYTOLOGY; AMNIOTIC FLUID CELL; ANAMNESIS; ANEUPLOIDY; ARTICLE; CASE REPORT; CELL CULTURE; CHROMOSOME 21; CHROMOSOME ANALYSIS; CLINICAL OBSERVATION; CONCEPTION; CYTOGENETICS; DNA ISOLATION; FAMILIAL DISEASE; FAMILY; FEMALE; FETUS; GENE AMPLIFICATION; GENETIC COUNSELING; HOMOZYGOSITY; HUMAN; KARYOTYPE; KARYOTYPING; MEDICAL INFORMATION; MICROSATELLITE MARKER; MOLECULAR BIOLOGY; PATIENT INFORMATION; PATIENT REFERRAL; PREGNANCY; PREGNANCY TERMINATION; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; RECURRENT DISEASE; SAMPLE; SUPERNUMERARY CHROMOSOME; TRISOMY 21; UNIPARENTAL DISOMY; UNIPARENTAL DISOMY 21;

ADULT; ALLELES; CHROMOSOMES, HUMAN, PAIR 21; DOWN SYNDROME; FEMALE; FETAL DISEASES; HUMANS; MALE; PEDIGREE; PREGNANCY; PRENATAL DIAGNOSIS; UNIPARENTAL DISOMY;

EID: 18244413336     PISSN: 10153837     EISSN: None     Source Type: Journal    
DOI: 10.1159/000073142     Document Type: Article

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