McFadden DE - Search Results

1

Renal tubular dysgenesis with calvarial hypoplasia: report of two additional cases and review.

McFadden DE, Pantzar JT, Van Allen MI, Langlois S. McFadden DE, et al. J Med Genet. 1997 Oct;34(10):846-8. doi: 10.1136/jmg.34.10.846. J Med Genet. 1997. PMID: 9350819 Free PMC article.

2

The impact of prenatal diagnosis on neural tube defect (NTD) pregnancy versus birth incidence in British Columbia.

Van Allen MI, Boyle E, Thiessen P, McFadden D, Cochrane D, Chambers GK, Langlois S, Stathers P, Irwin B, Cairns E, MacLeod P, Delisle MF, Uh SH. Van Allen MI, et al. J Appl Genet. 2006;47(2):151-8. doi: 10.1007/BF03194615. J Appl Genet. 2006. PMID: 16682757

3

Renal-hepatic-pancreatic dysplasia: an autosomal recessive condition that is not linked to the PKHD1 gene on chromosome 6p21.1-p12.

Schrader KA, Nelson TN, McFadden DE, Pantzar T, Langlois S. Schrader KA, et al. Among authors: mcfadden de. Am J Med Genet A. 2007 Aug 1;143A(15):1806-8. doi: 10.1002/ajmg.a.31818. Am J Med Genet A. 2007. PMID: 17593545 No abstract available.

4

Parental origin of triploidy in human fetuses: evidence for genomic imprinting.

McFadden DE, Kwong LC, Yam IY, Langlois S. McFadden DE, et al. Hum Genet. 1993 Nov;92(5):465-9. doi: 10.1007/BF00216452. Hum Genet. 1993. PMID: 7902318

5

Placental pathology of triploidy.

McFadden DE, Pantzar JT. McFadden DE, et al. Hum Pathol. 1996 Oct;27(10):1018-20. doi: 10.1016/s0046-8177(96)90277-4. Hum Pathol. 1996. PMID: 8892584

6

Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: sex specific differences.

Mitchell J, Schinzel A, Langlois S, Gillessen-Kaesbach G, Schuffenhauer S, Michaelis R, Abeliovich D, Lerer I, Christian S, Guitart M, McFadden DE, Robinson WP. Mitchell J, et al. Among authors: mcfadden de. Am J Med Genet. 1996 Oct 16;65(2):133-6. doi: 10.1002/(SICI)1096-8628(19961016)65:2<133::AID-AJMG10>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8911605

7

Gonadal pathology in triploidy.

McFadden DE, Pantzar JT, Jevon GP. McFadden DE, et al. Pediatr Dev Pathol. 2000 Nov-Dec;3(6):548-55. doi: 10.1007/s100240010114. Pediatr Dev Pathol. 2000. PMID: 11000332

8

Parental and meiotic origin of triploidy in the embryonic and fetal periods.

McFadden DE, Langlois S. McFadden DE, et al. Clin Genet. 2000 Sep;58(3):192-200. doi: 10.1034/j.1399-0004.2000.580306.x. Clin Genet. 2000. PMID: 11076041

9

The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders.

Bourque DK, Peñaherrera MS, Yuen RK, Van Allen MI, McFadden DE, Robinson WP. Bourque DK, et al. Among authors: mcfadden de. Clin Genet. 2011 Feb;79(2):169-75. doi: 10.1111/j.1399-0004.2010.01443.x. Clin Genet. 2011. PMID: 20507345

10

Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism.

Robinson WP, McFadden DE, Barrett IJ, Kuchinka B, Peñaherrera MS, Bruyère H, Best RG, Pedreira DA, Langlois S, Kalousek DK. Robinson WP, et al. Among authors: mcfadden de. Prenat Diagn. 2002 Dec;22(12):1076-85. doi: 10.1002/pd.483. Prenat Diagn. 2002. PMID: 12454962

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