A FISH probe specific for the telomeric region of 6p. by Mirza, G, Davies, A, Ragoussis, I

Partial trisomy 22 in a liveborn resulting from a rearrangement between chromosomes 6 and 22. by Mirza, G, Imaizumi, K, Ragoussis, J

An interstitial deletion of 6p24-p25 proximal to the FKHL7 locus and including AP-2alpha that affects anterior eye chamber development. by Davies, A, Mirza, G, Flinter, F, Ragoussis, J

Genomic sequencing and transcript identification over a 700kb region in human 6p24 containing three translocation breakpoints associated with orofacial clefting. by Ragoussis, J, Knaggs, S, Mirza, G, Macris, I, Stephens, R, Mungall, A

A serpin gene cluster on human chromosome 6p25 contains PI6, PI9 and ELANH2 which have a common structure almost identical to the 18q21 ovalbumin serpin genes. by Sun, J, Stephens, R, Mirza, G, Kanai, H, Ragoussis, J, Bird, P

Mapping of three translocation breakpoints associated with orofacial clefting within 6p24 and identification of new transcripts within the region. by Davies, S, Wise, C, Venkatesh, B, Mirza, G, Jefferson, A, Volpi, E, Ragoussis, J

Schizophrenia in an adult with 6p25 deletion syndrome. by Caluseriu, O, Mirza, G, Ragoussis, J, Chow, E, MacCrimmon, D, Bassett, A

Molecular cloning, chromosomal mapping, and developmental expression of a novel protein tyrosine phosphatase-like gene. by Uwanogho, D, Hardcastle, Z, Balogh, P, Mirza, G, Thornburg, K, Ragoussis, J, Sharpe, P

Further evidence for the involvement of human chromosome 6p24 in the aetiology of orofacial clefting. by Davies, A, Imaizumi, K, Mirza, G, Stephens, R, Kuroki, Y, Matsuno, M, Ragoussis, J

Molecularly defined interstitial tandem duplication 6p case with mild manifestations. by Ng, D, Mowrey, P, Ragoussis, J, Mirza, G, Coll, E, Fazio, D, Turner, C, Levin, S

Refined genotype-phenotype correlations in cases of chromosome 6p deletion syndromes. by Mirza, G, Williams, R, Mohammed, S, Clark, R, Newbury-Ecob, R, Baldinger, S, Flinter, F, Ragoussis, J

A functional genomics approach to the investigation of human 6p gene function by Bogani, D, Kaur, K, Davies, J, Mirza, G, Willoughby, C, Mckeone, R, Denny, P, Ragoussis, J, Arkell, R

A statistical approach for detecting genomic aberrations in heterogeneous tumor samples from single nucleotide polymorphism genotyping data. by Yau, C, Mouradov, D, Jorissen, R, Colella, S, Mirza, G, Steers, G, Harris, A, Ragoussis, J, Sieber, O, Holmes, C

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data by Colella, S, Yau, C, Taylor, J, Mirza, G, Butler, H, Clouston, P, Bassett, A, Seller, A, Holmes, C, Ragoussis, J

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data. by Colella, S, Yau, C, Taylor, J, Mirza, G, Butler, H, Clouston, P, Bassett, A, Seller, A, Holmes, C, Ragoussis, J

Detailed characterisation of six cases with 6p deletions by FISH; delineation of the syndrome. by Ragoussis, J, Davies, A, Mirza, G, Olavesen, MG, Stephens, R, Sekhon, G, Turnpenny, P, Leroy, F, Speleman, F, Flinter, F

Human epidermal differentiation complex in a single 2.5 Mbp long continuum of overlapping DNA cloned in bacteria integrating physical and transcript maps. by South, A, Cabral, A, Ives, J, James, C, Mirza, G, Marenholz, I, Mischke, D, Backendorf, C, Ragoussis, J, Nizetic, D

Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population. by Villanueva, P, Newbury, D, Jara, L, De Barbieri, Z, Mirza, G, Palomino, H, Fernández, M, Cazier, J, Monaco, A, Palomino, H

Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population by Villanueva, P, Newbury, D, Jara, L, De Barbieri, Z, Mirza, G, Palamino, H, Fernández, M, Cazier, J, Monaco, A, Palomino, H

Delineation of two distinct 6p deletion syndromes. by Davies, A, Mirza, G, Sekhon, G, Turnpenny, P, Leroy, F, Speleman, F, Law, C, van Regemorter, N, Vamos, E, Flinter, F, Ragoussis, J