Davies AF - Search Results

1

A fetus with an X;1 balanced reciprocal translocation and eye disease.

Seller MJ, Pal K, Horsley S, Davies AF, Berry AC, Meredith R, McCartney AC. Seller MJ, et al. Among authors: davies af. J Med Genet. 1995 Jul;32(7):557-60. doi: 10.1136/jmg.32.7.557. J Med Genet. 1995. PMID: 7562972 Free PMC article.

2

A 46,XX fetus with external female and internal male genitalia, facial dysmorphic features and mildly dilated lateral ventricles of the brain: a new syndrome?

Becker K, Seller MJ, Pal K, Davies AF. Becker K, et al. Among authors: davies af. Clin Dysmorphol. 2001 Jul;10(3):215-7. doi: 10.1097/00019605-200107000-00012. Clin Dysmorphol. 2001. PMID: 11446417

3

Further evidence for the involvement of human chromosome 6p24 in the aetiology of orofacial clefting.

Davies AF, Imaizumi K, Mirza G, Stephens RS, Kuroki Y, Matsuno M, Ragoussis J. Davies AF, et al. J Med Genet. 1998 Oct;35(10):857-61. doi: 10.1136/jmg.35.10.857. J Med Genet. 1998. PMID: 9783713 Free PMC article.

4

An interstitial deletion of 6p24-p25 proximal to the FKHL7 locus and including AP-2alpha that affects anterior eye chamber development.

Davies AF, Mirza G, Flinter F, Ragoussis J. Davies AF, et al. J Med Genet. 1999 Sep;36(9):708-10. J Med Genet. 1999. PMID: 10507730 Free PMC article.

5

FISH detection of trisomy 21 in interphase by the simultaneous use of two differentially labelled cosmid contigs.

Davies AF, Barber L, Murer-Orlando M, Bobrow M, Adinolfi M. Davies AF, et al. J Med Genet. 1994 Sep;31(9):679-85. doi: 10.1136/jmg.31.9.679. J Med Genet. 1994. PMID: 7815435 Free PMC article.

6

A pericentric inversion of chromosome six in a patient with Peutz-Jeghers' syndrome and the use of FISH to localise the breakpoints on a genetic map.

Markie D, Huson S, Maher E, Davies A, Tomlinson I, Bodmer WF. Markie D, et al. Hum Genet. 1996 Aug;98(2):125-8. doi: 10.1007/s004390050173. Hum Genet. 1996. PMID: 8698325

7

Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region.

Davies AF, Stephens RJ, Olavesen MG, Heather L, Dixon MJ, Magee A, Flinter F, Ragoussis J. Davies AF, et al. Hum Mol Genet. 1995 Jan;4(1):121-8. doi: 10.1093/hmg/4.1.121. Hum Mol Genet. 1995. PMID: 7711723

8

A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome.

Davies AF, Olavesen MG, Stephens RJ, Davidson R, Delneste D, Van Regemorter N, Vamos E, Flinter F, Abusaad I, Ragoussis J. Davies AF, et al. Hum Genet. 1996 Oct;98(4):454-9. doi: 10.1007/s004390050239. Hum Genet. 1996. PMID: 8792822

9

Delineation of an estimated 6.7 MB candidate interval for an anophthalmia gene at 3q26.33-q28 and description of the syndrome associated with visible chromosome deletions of this region.

Male A, Davies A, Bergbaum A, Keeling J, FitzPatrick D, Mackie Ogilvie C, Berg J. Male A, et al. Eur J Hum Genet. 2002 Dec;10(12):807-12. doi: 10.1038/sj.ejhg.5200890. Eur J Hum Genet. 2002. PMID: 12461687

10

Deletion of the distal long arm of chromosome 10; is there a characteristic phenotype? A report of 15 de novo and familial cases.

Irving M, Hanson H, Turnpenny P, Brewer C, Ogilvie CM, Davies A, Berg J. Irving M, et al. Am J Med Genet A. 2003 Dec 1;123A(2):153-63. doi: 10.1002/ajmg.a.20220. Am J Med Genet A. 2003. PMID: 14598339

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