Prenatal diagnosis of de novo (7;19)(q11.2;q13.3) translocation associated with a thick corpus callosum and Wilms tumor of the kidneys

Prenatal Diagnosis

Volumn 25, Issue 10, 2005, Pages 876-878

  Cavicchioni, Ottavia ^a   Gomes, Denise Molina ^b   Leroy, Brigitte ^b   Vialard, François ^b   Hillion, Yvette ^b   Selva, Jacqueline ^b   Ville, Yves ^a  

^a University of Paris Ouest   (France)

^b CENTRE HOSPITALIER INTERCOMMUNAL   (France)

Author keywords

Corpus callosum; De novo (7; 19) translocation; Prenatal diagnosis; Wilms tumor

Indexed keywords

ADULT; ARTICLE; AUTOPSY; CASE REPORT; CEREBELLUM VERMIS; CHROMOSOME 7; CHROMOSOME 9; CHROMOSOME TRANSLOCATION; CISTERNA MAGNA; CORPUS CALLOSUM; FEMALE; FETUS; HUMAN; HUMAN TISSUE; KARYOTYPE; LOW SET EAR; MICROGNATHIA; MICROTIA; NEPHROBLASTOMA; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; ULTRASOUND;

ABNORMALITIES, MULTIPLE; ADULT; CHROMOSOMES, HUMAN, PAIR 19; CHROMOSOMES, HUMAN, PAIR 7; CORPUS CALLOSUM; CRANIOFACIAL ABNORMALITIES; FEMALE; GESTATIONAL AGE; HUMANS; KARYOTYPING; KIDNEY NEOPLASMS; PREGNANCY; PRENATAL DIAGNOSIS; TRANSLOCATION, GENETIC; WILMS TUMOR;

MICROTIA;

EID: 27144519664     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.1129     Document Type: Article

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