AAAAAA
Results:
1-8
|
Results: 8
Authors:
Joyce, CA
Dennis, NR
Cooper, S
Browne, CE
Citation: Ca. Joyce et al., Subtelomeric rearrangements: results from a study of selected and unselected probands with idiopathic mental retardation and control individuals by using high-resolution G-banding and FISH, HUM GENET, 109(4), 2001, pp. 440-451
Authors:
Bolton, PF
Dennis, NR
Browne, CE
Thomas, NS
Veltman, MWM
Thompson, RJ
Jacobs, P
Citation: Pf. Bolton et al., The phenotypic manifestations of interstitial duplications of proximal 15qwith special reference to the autistic spectrum disorders, AM J MED G, 105(8), 2001, pp. 675-685
Authors:
Murray, A
Ennis, S
Youings, SA
Sharrock, AJ
Lewis, C
Pound, MC
Macpherson, JN
Dennis, NR
Morton, NE
Jacobs, PA
Citation: A. Murray et al., Stability and haplotype analysis of the FRAXE region, EUR J HUM G, 8(8), 2000, pp. 583-589
Authors:
Hammans, SR
Robinson, DO
Moutou, C
Kennedy, CR
Dennis, NR
Hughes, PJ
Ellison, DW
Citation: Sr. Hammans et al., A clinical and genetic study of a manifesting heterozygote with X-linked myotubular myopathy, NEUROMUSC D, 10(2), 2000, pp. 133-137
Authors:
Turner, C
Dennis, NR
Skuse, DH
Jacobs, PA
Citation: C. Turner et al., Seven ring (X) chromosomes lacking the XIST locus, six with an unexpectedly mild phenotype, HUM GENET, 106(1), 2000, pp. 93-100
Authors:
Marsh, AJ
Wellesley, D
Burge, D
Ashton, M
Browne, CE
Dennis, NR
Temple, IK
Citation: Aj. Marsh et al., Interstitial deletion of chromosome 17 (del(17)(q22q23.3)) confirms a linkwith oesophageal atresia, J MED GENET, 37(9), 2000, pp. 701-704
Authors:
Thomas, NS
Sharp, AJ
Browne, CE
Skuse, D
Hardie, C
Dennis, NR
Citation: Ns. Thomas et al., Xp deletions associated with autism in three females, HUM GENET, 104(1), 1999, pp. 43-48
Authors:
Joyce, CA
Ross, FM
Dennis, NR
Wyre, ND
Barber, JCK
Citation: Ca. Joyce et al., Multipaint FISH: a rapid and reliable way to define cryptic and complex abnormalities, CLIN GENET, 56(3), 1999, pp. 192-199
Risultati:
1-8
|