Twin pregnancy with a chimeric androgenetic and biparental placenta in one twin displaying placental mesenchymal dysplasia phenotype.

Three-dimensional sonography of placental mesenchymal dysplasia and its differential diagnosis. J Ultrasound Med (2009) 1.20

Pregnancy with concomitant chorioangioma and placental mesenchymal dysplasia: a rare placental abnormality. Case Rep Obstet Gynecol (2013) 0.90

Mosaics and moles. Eur J Hum Genet (2011) 0.83

Zygotes segregate entire parental genomes in distinct blastomere lineages causing cleavage-stage chimerism and mixoploidy. Genome Res (2016) 0.79

Paternal Hemizygosity in 11p15 in Mole-like Conceptuses: Two Case Reports. Medicine (Baltimore) (2015) 0.75

Evaluation of fetuses in a study of intravenous immunoglobulin as preventive therapy for congenital heart block: Results of a multicenter, prospective, open-label clinical trial. Arthritis Rheum (2010) 1.52

Society for fetal urology recommendations for postnatal evaluation of prenatal hydronephrosis--will fewer voiding cystourethrograms lead to more urinary tract infections? J Urol (2013) 1.46

Whole exome sequencing in a random sample of North American women with leiomyomas identifies MED12 mutations in majority of uterine leiomyomas. PLoS One (2012) 1.43

NLRP7 in the spectrum of reproductive wastage: rare non-synonymous variants confer genetic susceptibility to recurrent reproductive wastage. J Med Genet (2011) 1.04

Paternal origins of complete hydatidiform moles proven by whole genome single-nucleotide polymorphism haplotyping. Genomics (2002) 1.01

The timing of delivery of infants with gastroschisis influences outcome. J Pediatr Surg (2005) 1.00

P57KIP2 immunostaining and molecular cytogenetics: combined approach aids in diagnosis of morphologically challenging cases with molar phenotype and in detecting androgenetic cell lines in mosaic/chimeric conceptions. Hum Pathol (2007) 0.93

The origin of trisomy 22: evidence for acrocentric chromosome-specific patterns of nondisjunction. Am J Med Genet A (2007) 0.91

The origin of trisomy 13. Am J Med Genet A (2007) 0.91

Risk of morbid perinatal outcomes in small-for-gestational-age pregnancies: customized compared with conventional standards of fetal growth. Obstet Gynecol (2012) 0.89

Massively parallel sequencing of maternal plasma DNA in 113 cases of fetal nuchal cystic hygroma. Obstet Gynecol (2013) 0.87

Transvaginal ultrasound measurement of endometrial thickness as a biomarker for estrogen exposure. Cancer Epidemiol Biomarkers Prev (2004) 0.84

Prenatal diagnosis of trisomy 6 rescue resulting in paternal UPD6 with novel placental findings. Am J Med Genet A (2011) 0.81

Persistent gestational trophoblastic disease after an androgenetic/biparental fetal chimera: a case report and review. Int J Gynecol Pathol (2006) 0.78

Complex X chromosome rearrangement delineated by array comparative genome hybridization in a woman with premature ovarian insufficiency. Fertil Steril (2011) 0.78

Prenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype. Prenat Diagn (2012) 0.78

Sonographic biometry in the early third trimester: A comparison of parameters to predict macrosomia at birth. J Clin Ultrasound (2014) 0.77

Sonographic detection of gallbladder duplication: two cases discovered in utero. J Ultrasound Med (2002) 0.77

Accuracy of prenatal diagnosis of isolated aqueductal stenosis. Prenat Diagn (2015) 0.76

Endometrial thickness and risk of breast and endometrial carcinomas in the prostate, lung, colorectal and ovarian cancer screening trial. Int J Cancer (2013) 0.76

Clinical report: Two patients with atelosteogenesis type I caused by missense mutations affecting the same FLNB residue. Am J Med Genet A (2013) 0.75

Radiology corner. Answer to last month's radiology case (# 44) and image: lithopedion. Mil Med (2010) 0.75

Anomalies of the forebrain with radial limb defects: Garcia-Lurie-Steinfeld syndrome? Birth Defects Res A Clin Mol Teratol (2004) 0.75

Longitudinal assessment of amniotic fluid volume in monoamniotic twin gestations. Prenat Diagn (2013) 0.75

Prenatal diagnosis of lower urinary tract obstruction associated with penoscrotal transposition. Prenat Diagn (2009) 0.75

Genomic Characterization of a Metastatic Alveolar Rhabdomyosarcoma Case Using FISH Studies and CGH+SNP Microarray Revealing FOXO1-PAX7 Rearrangement with MYCN and MDM2 Amplification and RB1 Region Loss. Cytogenet Genome Res (2017) 0.75

Fetal complete common atrioventricular canal defect: spontaneous closure of the ventricular septal defect--in utero anatomic evolution and postnatal outcomes. World J Pediatr Congenit Heart Surg (2013) 0.75