Parental and meiotic origin of triploidy in the embryonic and fetal periodsMCFADDEN, D. E; LANGLOIS, S.Clinical genetics. 2000, Vol 58, Num 3, pp 192-200, issn 0009-9163Article

Parental origin of triploidy in human fetuses : evidence for genomic imprintingMCFADDEN, D. E; KWONG, L. C; YAM, I. Y. L et al.Human genetics. 1993, Vol 92, Num 5, pp 465-469, issn 0340-6717Article

Teratoid Wilm's tumour : a report of two casesMAGEE, J. F; ANSARI, S; MCFADDEN, D. E et al.Histopathology. 1992, Vol 20, Num 5, pp 427-431, issn 0309-0167Article

Overlapping DNA methylation profile between placentas with trisomy 16 and early-onset preeclampsiaBLAIR, J. D; LANGLOIS, S; MCFADDEN, D. E et al.Placenta (Eastbourne). 2014, Vol 35, Num 3, pp 216-222, issn 0143-4004, 7 p.Article

Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome : Sex specific differencesMITCHELL, J; SCHINZEL, A; MCFADDEN, D. E et al.American journal of medical genetics. 1996, Vol 65, Num 2, pp 133-136, issn 0148-7299Article

Toll-like receptor 4 polymorphisms and idiopathic chromosomally normal miscarriageHIRSCHFELD, A. F; JIANG, R; ROBINSON, W. P et al.Human reproduction (Oxford. Print). 2007, Vol 22, Num 2, pp 440-443, issn 0268-1161, 4 p.Article

A novel ETV6-NTRK3 gene fusion in congenital fibrosarcomaKNEZEVICH, S. R; MCFADDEN, D. E; WEN TAO et al.Nature genetics. 1998, Vol 18, Num 2, pp 184-187, issn 1061-4036Article

Placental pathology of triploidyMCFADDEN, D. E; TAPIO PANTZAR, J. T.Human pathology. 1996, Vol 27, Num 10, pp 1018-1020, issn 0046-8177Article

Peritoneal inclusion cysts with mural mesothelial proliferation: a clinicopathological analysis of six casesMCFADDEN, D. E; CLEMENT, P. B.The American journal of surgical pathology. 1986, Vol 10, Num 12, pp 844-854, issn 0147-5185Article

The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disordersBOURQUE, D. K; PENAHERRERA, M. S; YUEN, Rkc et al.Clinical genetics. 2011, Vol 79, Num 2, pp 169-175, issn 0009-9163, 7 p.Article

Placental mesenchymal dysplasia associated with fetal overgrowth and mosaic deletion of the maternal copy of 11p15.5ROBINSON, W. P; SLEE, J; SMITH, N et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 15, pp 1752-1759, issn 1552-4825, 8 p.Article

Confirmation of prenatal diagnosis of sex chromosome mosaicismMCFADDEN, D. E; KALOUSEK, D. K.American journal of medical genetics. 1989, Vol 32, Num 4, pp 495-497, issn 0148-7299Article

Hypercalcemia associated with small cell anaplastic carcinoma of the rectumNANJI, A. A; MCFADDEN, D. E; OWEN, D. A et al.American journal of proctology, gastroenterology & colon & rectal surgery. 1984, Vol 35, Num 11, pp 7-14, issn 0162-6566, 3 p.Article

Androgenetic/biparental mosaicism causes placental mesenchymal dysplasiaKAISER-ROGERS, K. A; MCFADDEN, D. E; LIVASY, C. A et al.Journal of medical genetics. 2006, Vol 43, Num 2, pp 187-192, issn 0022-2593, 6 p.Article

The origin of abnormalities in recurrent aneuploidy/polyploidyROBINSON, W. P; MCFADDEN, D. E; STEPHENSON, M. D et al.American journal of human genetics. 2001, Vol 69, Num 6, pp 1245-1254, issn 0002-9297Article

Pleural relapse during hematopoietic remission in childhood acute lymphoblastic leukemiaDIX, D. B; ANDERSON, R. A; MCFADDEN, D. E et al.Journal of pediatric hematology/oncology. 1997, Vol 19, Num 5, pp 470-472, issn 1077-4114Article

Chromosome abnormalities in human beingsMCFADDEN, D. E; FRIEDMAN, J. M.Mutation research. 1997, Vol 396, Num 1-2, pp 129-140, issn 0027-5107Article

Phenotype of triploid embryosMCFADDEN, D. E; ROBINSON, W. P.Journal of medical genetics. 2006, Vol 43, Num 7, pp 609-612, issn 0022-2593, 4 p.Article

Two different phenotypes of fetuses with chromosomal triploidy : correlation with parental origin of the extra haploid setMCFADDEN, D. E; HALOUSEK, D. K.American journal of medical genetics. 1991, Vol 38, Num 4, pp 535-538, issn 0148-7299Article

Survey of neural tube defects in spontaneously aborted embryosMCFADDEN, D. E; KALOUSEK, D. K.American journal of medical genetics. 1989, Vol 32, Num 3, pp 356-358, issn 0148-7299, 3 p.Article

Frequency of meiotic trisomy depends on involved chromosome and mode of ascertainmentROBINSON, W. P; BERNASCONI, F; LAU, A et al.American journal of medical genetics. 1999, Vol 84, Num 1, pp 34-42, issn 0148-7299Article

Renal tubular dysgenesis with calvarial hypoplasia : report of two additional cases and reviewMCFADDEN, D. E; PANTZAR, J. T; VAN ALLEN, M. I et al.Journal of medical genetics. 1997, Vol 34, Num 10, pp 846-848, issn 0022-2593Article

Precise localisation of 3p25 breakpoints in four patients with the 3p- syndromeDRUMHELLER, T; MCGILLIVRAY, B. C; BEHRNER, D et al.Journal of medical genetics. 1996, Vol 33, Num 10, pp 842-847, issn 0022-2593Article