Post-zygotic origin of isochromosome 12p

Prenatal Diagnosis

Volumn 24, Issue 12, 2004, Pages 984-988

  De Ravel, Thomy J L ^a,d   Keymolen, Kathelijn ^b   Van Assche, Elvire ^b   Wittevronghel, Ingrid ^c   Moerman, Philippe ^a   Salden, Ivo ^a   Matthijs, Gert ^a   Fryns, Jean Pierre ^a   Vermeesch, Joris R ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b VRIJE UNIVERSITEIT BRUSSEL   (Belgium)

^c Algemeen Ziekenhuis Sint Maarten   (Belgium)

^d UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

Isochromosome 12p; Pallister Killian syndrome; Trisomy 12

Indexed keywords

AMNION CELL; ARTICLE; CASE REPORT; CELL CULTURE; CHROMOSOME 12P; CHROMOSOME BANDING PATTERN; CHROMOSOME G BAND; DNA DETERMINATION; FEMALE; FETUS; FETUS ECHOGRAPHY; FIBROBLAST; FLUORESCENCE IN SITU HYBRIDIZATION; GENE PROBE; HUMAN; HUMAN TISSUE; ISOCHROMOSOME; ISOCHROMOSOME 12P; KARYOTYPE 46,XX; KARYOTYPE 47,XX; PALLISTER KILLIAN SYNDROME; PRIORITY JOURNAL; TELOMERE;

ADULT; ALLELES; AMNIOTIC FLUID; CELLS, CULTURED; CHORIONIC VILLI; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 12; DNA; FEMALE; FIBROBLASTS; GESTATIONAL AGE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; ISOCHROMOSOMES; KARYOTYPING; PREGNANCY; PRENATAL DIAGNOSIS; ZYGOTE;

EID: 10844295808     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.956     Document Type: Article

References (13)

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