Reproductive consequences of genome-wide paternal uniparental disomy mosaicism: description of two cases with different mechanisms of origin and pregnancy outcomes

Fertility and Sterility

Volumn 92, Issue 1, 2009, Pages 393.e5-393.e9

  Morales, Carme ^a,c   Soler, Anna ^a,c,d   Badenas, Cèlia ^a,c,d   Rodríguez Revenga, Laia ^c   Nadal, Alfons ^b   Martínez, José M ^a,d   Mademont Soler, Irene ^a   Borrell, Antoni ^a,c,d   Milà, Montserrat ^a,c,d   Sánchez, Aurora ^a,c,d  

^a HOSPITAL CLÍNIC   (Spain)

^b Hospitals Universitaris Vall d'H   (Spain)

^c CENTRO DE INVESTIGACIÓN BIOMÉDICA EN RED DE ENFERMEDADES RARAS CIBERER   (Spain)

^d INSTITUT D INVESTIGACIONS BIOMÈDIQUES AUGUST PI I SUNYER IDIBAPS   (Spain)

Author keywords

Androgenetic; Beckwith Wiedemann syndrome; genome wide paternal UPD; mosaicism; placental mesenchymal dysplasia; QF PCR

Indexed keywords

ADULT; ARTICLE; BECKWITH WIEDEMANN SYNDROME; CASE REPORT; CYTOGENETICS; ECHOGRAPHY; FEMALE; FERTILIZATION; FETUS MALFORMATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC COUNSELING; HUMAN; HYDRAMNIOS; INHERITANCE; KARYOTYPING; MOSAICISM; PATERNAL UNIPARENTAL DISOMY; PLACENTA DISORDER; PLACENTAL MESENCHYMAL DYSPLASIA; POLYMERASE CHAIN REACTION; PREGNANCY OUTCOME; PRIORITY JOURNAL; UNIPARENTAL DISOMY;

EID: 67649126211     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fertnstert.2009.03.090     Document Type: Article

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