Utility of microsatellite analysis in evaluation of pregnancies with placental mesenchymal dysplasia

To demonstrate a role for microsatellite analysis in the evaluation of prenatal cases with possible placental mesenchymal dysplasia (PMD).

[1]  K. Benirschke,et al.  Placental Mesenchymal Dysplasia Is Associated With High Rates of Intrauterine Growth Restriction and Fetal Demise , 2006 .

[2]  R. Mao,et al.  Molecular diagnosis of Prader-Willi and Angelman syndromes by methylation-specific melting analysis and methylation-specific multiplex ligation-dependent probe amplification. , 2006, Clinical chemistry.

[3]  R. Kuick,et al.  Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans , 2006, Nature Genetics.

[4]  U. Surti,et al.  Twin pregnancy with a chimeric androgenetic and biparental placenta in one twin displaying placental mesenchymal dysplasia phenotype , 2005, Prenatal diagnosis.

[5]  C. Livasy,et al.  Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia , 2005, Journal of Medical Genetics.

[6]  N. Sebire,et al.  Placental mesenchymal dysplasia associated with fetal aneuploidy , 2005, Prenatal diagnosis.

[7]  E. S. Suarez,et al.  Mesenchymal dysplasia of the placenta. , 2004, Placenta.

[8]  A. Sampson,et al.  Placental mesenchymal dysplasia: A report of four cases with differentiation from partial hydatidiform mole , 2003, The Australian & New Zealand journal of obstetrics & gynaecology.

[9]  A. Mitsuhashi,et al.  Placental mesenchymal dysplasia initially diagnosed as partial mole , 2003, Pathology international.

[10]  A. Prusa,et al.  Amniotic fluid cells and human stem cell research: a new connection. , 2002, Medical science monitor : international medical journal of experimental and clinical research.

[11]  N. Sebire,et al.  Complete hydatidiform mole and normal live birth: a novel case of confined placental mosaicism: case report. , 2002, Human reproduction.

[12]  R. Weksberg,et al.  Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1. , 2001, Human molecular genetics.

[13]  N. Sebire,et al.  Pseudo‐partial moles: placental stem vessel hydrops and the association with Beckwith–Wiedemann syndrome and complete moles , 2001, Histopathology.

[14]  M. Vazquez,et al.  Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith–Wiedemann syndrome , 2001, European Journal of Human Genetics.

[15]  J. Ruijter,et al.  Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS. , 2001, Human molecular genetics.

[16]  Yukichi Tanaka,et al.  Mesenchymal dysplasia of the placenta , 2000, Pathology international.

[17]  K. Nicolaides,et al.  Investigation of the cause of miscarriage and its influence on women's psychological distress , 1999, British journal of obstetrics and gynaecology.

[18]  R. Franche,et al.  The impact of perinatal loss on adjustment to subsequent pregnancy. , 1999, Social science & medicine.

[19]  K. Nicolaides,et al.  Perinatal features associated with placental mesenchymal dysplasia. , 1997, Placenta.

[20]  A R Zinsmeister,et al.  Dynamics of chromosome spreading. , 1996, American journal of medical genetics.

[21]  R. Berkowitz,et al.  Natural history of twin pregnancy with complete hydatidiform mole and coexisting fetus , 1994, Obstetrics and gynecology.

[22]  M. Leader,et al.  Partial hydatidiform mole: a common but underdiagnosed condition. A 3-year retrospective clinicopathological and DNA flow cytometric analysis. , 1993, International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.

[23]  J. Lage.  Placentomegaly with massive hydrops of placental stem villi, diploid DNA content, and fetal omphaloceles: possible association with Beckwith-Wiedemann syndrome. , 1991, Human pathology.

[24]  G. Dewald,et al.  Culturing and robotic harvesting of bone marrow, lymph nodes, peripheral blood, fibroblasts, and solid tumors with in situ techniques. , 1988, Cancer genetics and cytogenetics.