McFadden D - Search Results

1

Schinzel-Giedion syndrome: report of splenopancreatic fusion and proposed diagnostic criteria.

Lehman AM, McFadden D, Pugash D, Sangha K, Gibson WT, Patel MS. Lehman AM, et al. Among authors: mcfadden d. Am J Med Genet A. 2008 May 15;146A(10):1299-306. doi: 10.1002/ajmg.a.32277. Am J Med Genet A. 2008. PMID: 18398855

2

Anterolateral diaphragmatic hernia with body wall defect understood in relation to the abaxial domain.

Lehman AM, Cowan JR, McFadden DE, Patel MS. Lehman AM, et al. Am J Med Genet A. 2014 Jul;164A(7):1860-2. doi: 10.1002/ajmg.a.36529. Epub 2014 Apr 3. Am J Med Genet A. 2014. PMID: 24700809 No abstract available.

3

Phenotype of triploid embryos.

McFadden DE, Robinson WP. McFadden DE, et al. J Med Genet. 2006 Jul;43(7):609-12. doi: 10.1136/jmg.2005.037747. Epub 2005 Oct 19. J Med Genet. 2006. PMID: 16236813 Free PMC article.

4

Two different phenotypes of fetuses with chromosomal triploidy: correlation with parental origin of the extra haploid set.

McFadden DE, Kalousek DK. McFadden DE, et al. Am J Med Genet. 1991 Mar 15;38(4):535-8. doi: 10.1002/ajmg.1320380407. Am J Med Genet. 1991. PMID: 2063893

5

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.

6

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. 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.

7

Confirmation of prenatal diagnosis of sex chromosome mosaicism.

McFadden DE, Kalousek DK. McFadden DE, et al. Am J Med Genet. 1989 Apr;32(4):495-7. doi: 10.1002/ajmg.1320320413. Am J Med Genet. 1989. PMID: 2773991

8

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

9

Recurrent trisomy 15 in a female carrier of der(15)t(Y;15)(q12;p13).

Rajcan-Separovic E, Robinson WP, Stephenson M, Pantzar T, Arbour L, McFadden D, Guscott J. Rajcan-Separovic E, et al. Among authors: mcfadden d. Am J Med Genet. 2001 Apr 1;99(4):320-4. doi: 10.1002/1096-8628(2001)9999:9999<::aid-ajmg1173>3.0.co;2-1. Am J Med Genet. 2001. PMID: 11252000

10

Survey of neural tube defects in spontaneously aborted embryos.

McFadden DE, Kalousek DK. McFadden DE, et al. Am J Med Genet. 1989 Mar;32(3):356-8. doi: 10.1002/ajmg.1320320317. Am J Med Genet. 1989. PMID: 2786339

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