Mosaic trisomy 11 in a fetus with bilateral renal agenesis: Co-incidence or new association?

Clinical Dysmorphology

Volumn 20, Issue 1, 2011, Pages 47-49

  Balasubramanian, Meena ^a   Peres, Luiz Cesar ^a   Pelly, Dorothy ^a  

^a SHEFFIELD CHILDREN S HOSPITAL   (United Kingdom)

Author keywords

fetus; inner cell mass; mosaicism; post mortem; renal agenesis; uniparental disomy

Indexed keywords

ARTICLE; CASE REPORT; CYTOGENETICS; DISEASE ASSOCIATION; FETUS; FETUS DISEASE; FLATFOOT; GENETIC COUNSELING; HISTOLOGY; HUMAN; KARYOTYPE; KIDNEY AGENESIS; LUNG HYPOPLASIA; MALE; MOSAICISM; OLIGOHYDRAMNIOS; POTTER SYNDROME; PREGNANCY TERMINATION; PRIORITY JOURNAL; TRISOMY;

CHROMOSOMES, HUMAN, PAIR 11; FEMALE; FETUS; HUMANS; KIDNEY; MALE; MOSAICISM; PREGNANCY; TRISOMY;

EID: 78650799665     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/MCD.0b013e32833ff2e9     Document Type: Article

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