Placental Mesenchymal Dysplasia with Beckwith-Wiedemann Syndrome Fetus in the Context of Biparental and Androgenic Cell Lines

Placenta

Volumn 29, Issue 5, 2008, Pages 454-460

  H'mida, D ^a   Gribaa, M ^a   Yacoubi, T ^a   Chaieb, A ^a   Adala, L ^a   Elghezal, H ^a   Saad, A ^a  

^a FARHAT HACHED HOSPITAL   (Tunisia)

Author keywords

Beckwith Wiedemann syndrome; Double fertilisation; Paternal uniparental isodisomy; Placental mesenchymal dysplasia

Indexed keywords

DNA MARKER;

ADULT; ALLELE; ARTICLE; BECKWITH WIEDEMANN SYNDROME; CASE REPORT; CELL LINE; CELL PROLIFERATION; CLINICAL FEATURE; CYTOMEGALY; DIPLOIDY; FEMALE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ANALYSIS; HAPLOIDY; HEPATOMEGALY; HUMAN; HUMAN CELL; HUMAN TISSUE; PANCREAS ISLET; PHENOTYPE; PLACENTA DISORDER; PLACENTA VILLUS; PLACENTAL MESENCHYMAL DYSPLASIA; PRIORITY JOURNAL; TROPHOBLAST; UNIPARENTAL DISOMY;

ADULT; ANDROGENS; BECKWITH-WIEDEMANN SYNDROME; CELL LINE; CHIMERISM; FEMALE; FETUS; HUMANS; INHERITANCE PATTERNS; MESODERM; MODELS, BIOLOGICAL; PLACENTA DISEASES; PREGNANCY; PREGNANCY TRIMESTER, FIRST;

EID: 43049109810     PISSN: 01434004     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.placenta.2008.01.001     Document Type: Article

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