Prenatal diagnosis of a half-cryptic translocation using chromosome microdissection

Prenatal Diagnosis

Volumn 17, Issue 4, 1997, Pages 369-374

  Senger, G ^a   Chudoba, I ^a   Friedrich, U ^a,b   Tommerup, N ^c,d   Claussen, U ^a   Brondum Nielsen K ^c  

^a FRIEDRICH SCHILLER UNIVERSITY JENA   (Germany)

^b AARHUS UNIVERSITY   (Denmark)

^c JOHN F KENNEDY INSTITUTE   (Denmark)

^d UNIVERSITY OF COPENHAGEN   (Denmark)

Author keywords

15; 17 translocation; Chromosome microdissection; DOP; Prenatal diagnosis; Reverse painting

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 15; CHROMOSOME 15Q; CHROMOSOME 17; CHROMOSOME 17P; CHROMOSOME ABERRATION; CHROMOSOME INSERTION; CHROMOSOME MICRODISSECTION; CHROMOSOME TRANSLOCATION; CONTROLLED STUDY; FACE DYSMORPHIA; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; KARYOTYPE; MENTAL DEFICIENCY; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RECIPROCAL CHROMOSOME TRANSLOCATION;

ADULT; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 15; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; GENETIC TECHNIQUES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; PEDIGREE; POLYMERASE CHAIN REACTION; PREGNANCY; PRENATAL DIAGNOSIS; TRANSLOCATION, GENETIC;

EID: 0030942233     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199704)17:4<369::AID-PD33>3.0.CO;2-S     Document Type: Article

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