Molecular cytogenetic characterisation of an interstitial deletion 12p detected by prenatal diagnosis

Prenatal Diagnosis

Volumn 27, Issue 5, 2007, Pages 475-478

  Stumm, Markus ^a,b,e   Klopocki, Eva ^c   Gasiorek Wiens, Adam ^a   Knoll, Ute ^a   Wirjadi, Deni ^d   Sarioglu, Nanette ^c   Wegner, Rolf Dieter ^a,c   Tönnies, Holger ^c  

^a Zentrum fur Pranataldiagnostik   (Germany)

^b OTTO VON GUERICKE UNIVERSITY   (Germany)

^c CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^d Deutsch Türkische Gynäkologen Gesellschaft DTGG e V   (Germany)

^e Zentrum für Pränataldiagnostik   (Germany)

Author keywords

Array CGH; Chorionic villi sampling; Deletion 12p; Molecular cytogenetic analysis; Prenatal diagnosis

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHORION VILLUS SAMPLING; CHROMOSOME 12P; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME BAND; COMPARATIVE GENOMIC HYBRIDIZATION; DNA EXTRACTION; FEMALE; FETUS; FETUS DISEASE; FETUS ECHOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; GESTATIONAL AGE; GIEMSA STAIN; HUMAN; HUMAN CELL; HUMAN TISSUE; INTERSTITIAL CHROMOSOME DELETION; KARYOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; ABORTION; CHROMOSOME 12; CHROMOSOME DELETION; DIFFERENTIAL DIAGNOSIS; FIRST TRIMESTER PREGNANCY; GENETICS; MULTIPLE MALFORMATION SYNDROME; PREGNANCY; PRENATAL DEVELOPMENT; REVIEW;

ABNORMALITIES, MULTIPLE; ABORTION, EUGENIC; ADULT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 12; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; PREGNANCY; PREGNANCY TRIMESTER, FIRST; PRENATAL DIAGNOSIS;

EID: 34347270554     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1703     Document Type: Article

References (7)

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