Fagan K - Search Results

1

Paternal uniparental isodisomy for chromosome 14 with mosaicism for a supernumerary marker chromosome 14.

Mattes J, Whitehead B, Liehr T, Wilkinson I, Bear J, Fagan K, Craven P, Bennetts B, Edwards M. Mattes J, et al. Among authors: fagan k. Am J Med Genet A. 2007 Sep 15;143A(18):2165-71. doi: 10.1002/ajmg.a.31896. Am J Med Genet A. 2007. PMID: 17702046

2

Supernumerary ring chromosome 17 identified by fluorescent in situ hybridization.

Fagan K, Edwards M. Fagan K, et al. Am J Med Genet. 1997 Apr 14;69(4):352-5. Am J Med Genet. 1997. PMID: 9098481

3

A summary of 7q interstitial deletions and exclusion mapping of the gene for beta-glucuronidase.

Fagan K, Gill A, Henry R, Wilkinson I, Carey B. Fagan K, et al. J Med Genet. 1989 Oct;26(10):619-25. doi: 10.1136/jmg.26.10.619. J Med Genet. 1989. PMID: 2486209 Free PMC article.

4

The coagulation factor VII regulator is located on 8p23.1.

Fagan K, Wilkinson I, Allen M, Brownlea S. Fagan K, et al. Hum Genet. 1988 Aug;79(4):365-7. doi: 10.1007/BF00282178. Hum Genet. 1988. PMID: 3410461

5

An interstitial deletion of chromosome 7(q35).

Fagan K, Kennedy C, Roddick L, Colley A. Fagan K, et al. J Med Genet. 1994 Sep;31(9):738-9. doi: 10.1136/jmg.31.9.738. J Med Genet. 1994. PMID: 7529320 Free PMC article.

6

Translocations involving 4p16.3 in three families: deletion causing the Pitt-Rogers-Danks syndrome and duplication resulting in a new overgrowth syndrome.

Partington MW, Fagan K, Soubjaki V, Turner G. Partington MW, et al. Among authors: fagan k. J Med Genet. 1997 Sep;34(9):719-28. doi: 10.1136/jmg.34.9.719. J Med Genet. 1997. PMID: 9321756 Free PMC article.

7

Velo-cardio-facial and partial DiGeorge phenotype in a child with interstitial deletion at 10p13--implications for cytogenetics and molecular biology.

Lipson A, Fagan K, Colley A, Colley P, Sholler G, Issacs D, Oates RK. Lipson A, et al. Among authors: fagan k. Am J Med Genet. 1996 Nov 11;65(4):304-8. doi: 10.1002/(SICI)1096-8628(19961111)65:4<304::AID-AJMG11>3.0.CO;2-Y. Am J Med Genet. 1996. PMID: 8923940

8

A new interstitial deletion of 4q (q21.1::q22.1).

Fagan K, Gill A. Fagan K, et al. J Med Genet. 1989 Oct;26(10):644-7. doi: 10.1136/jmg.26.10.644. J Med Genet. 1989. PMID: 2585461 Free PMC article.

9

Anal anomalies: an uncommon feature of velocardiofacial (Shprintzen) syndrome?

Worthington S, Colley A, Fagan K, Dai K, Lipson AH. Worthington S, et al. Among authors: fagan k. J Med Genet. 1997 Jan;34(1):79-82. doi: 10.1136/jmg.34.1.79. J Med Genet. 1997. PMID: 9032655 Free PMC article.

10

FOXP1 mutations cause intellectual disability and a recognizable phenotype.

Le Fevre AK, Taylor S, Malek NH, Horn D, Carr CW, Abdul-Rahman OA, O'Donnell S, Burgess T, Shaw M, Gecz J, Bain N, Fagan K, Hunter MF. Le Fevre AK, et al. Among authors: fagan k. Am J Med Genet A. 2013 Dec;161A(12):3166-75. doi: 10.1002/ajmg.a.36174. Epub 2013 Sep 24. Am J Med Genet A. 2013. PMID: 24214399

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