Prenatal diagnosis of del(15)(q26.1) and del(18)(q21.3) due to an unbalanced de novo translocation: Ultrasound, molecular cytogenetic and autopsy findings

Prenatal Diagnosis

Volumn 20, Issue 12, 2000, Pages 992-995

  Leonard, Norma J ^a,b   Tomkins, Darrell J ^a   Demianczuk, Nestor ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

^b UNIVERSITY OF ALBERTA HOSPITAL   (Canada)

Author keywords

Bilateral renal agenesis; Potter sequence; Translocation 15; 18

Indexed keywords

ARTICLE; AUTOPSY; CHROMOSOME 15; CHROMOSOME 18; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION 15; CLINICAL FEATURE; CORDOCENTESIS; CYTOGENETICS; FETUS; FETUS ECHOGRAPHY; FETUS KARYOTYPING; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KIDNEY AGENESIS; OLIGOHYDRAMNIOS; POTTER SYNDROME; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

ADULT; CHROMOSOMES, HUMAN, PAIR 15; CHROMOSOMES, HUMAN, PAIR 18; FEMALE; GENE DELETION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; KIDNEY; PRENATAL DIAGNOSIS; SYNDROME; TRANSLOCATION, GENETIC; ULTRASONOGRAPHY, PRENATAL;

EID: 0034533264     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/1097-0223(200012)20:12<992::AID-PD950>3.0.CO;2-7     Document Type: Article

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3. Del(15)(q22q24) syndrome with Potter sequence
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6. Latent class analysis applied to patterns of fetal sonographic abnormalities: Definition of phenotypes associated with aneuploidy
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11. The 18q-syndrome: Analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-22.2
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14. Renal agenesis in British Columbia