A Paternally Inherited Duplication in the Prader-Willi/Angelman Syndrome Critical Region: A Case and Family Study von Veltman, Marijcke W. M, Thompson, Russell J, Craig, Ellen E, Dennis, Nicholas R, Roberts, Sian E, Moore, Vanessa, Brown, Josie A, Bolton, Patrick F

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Parental and chromosomal origins of microdeletion and duplication syndromes involving 7q11.23, 15q11-q13 and 22q11 von THOMAS, N. Simon, DURKIE, Miranda, POTTS, Gemma, SANDFORD, Richard, VAN ZYL, Berendine, YOUINGS, Sheila, DENNIS, Nicholas R, JACOBS, Patricia A

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Characterisation of interstitial duplications and triplications of chromosome 15q11-q13 von ROBERTS, Sian E, DENNIS, Nicholas R, BROWNE, Caroline E, WILLATT, Lionel, WOODS, C. Geoffrey, CROSS, Ian, JACOBS, Patricia A, THOMAS, N. Simon

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Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders von Bolton, Patrick F, Veltman, Marijcke W M, Weisblatt, Emma, Holmes, Joanne R, Thomas, N Simon, Youings, Sheila A, Thompson, Russell J, Roberts, Siân E, Dennis, Nicholas R, Browne, Caroline E, Goodson, Sally, Moore, Vanessa, Brown, Josie

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A familial balanced inverted insertion ins(15)(q15q13q11.2) producing Prader-Willi syndrome, Angelman syndrome and duplication of 15q11.2-q13 in a single family: Importance of diff... von Collinson, Morag N., Roberts, Siân E., Crolla, John A., Dennis, Nicholas R.

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An 11p;17p telomeric translocation in two families associated with recurrent miscarriages and Miller-Dieker syndrome von Joyce, Christine A, Dennis, Nicholas R, Howard, Francis, Davis, Louisa M, Thomas, N Simon

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Characterization of breakpoints in the GABRG3 and TSPY genes in a family with a t(Y;15)(p11.2;q12) von Gole, Leena, Crolla, John A., Thomas, Simon N., Jacobs, Patricia A., Dennis, Nicholas R.

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Multipaint FISH: a rapid and reliable way to define cryptic and complex abnormalities von Joyce, Christine A, Ross, Fiona M, Dennis, Nicholas R, Wyre, Nicholas D, Barber, John Ck

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Xp deletions associated with autism in three females von THOMAS, N. S, SHARP, A. J, BROWNE, C. E, SKUSE, D, HARDIE, C, DENNIS, N. R

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Interstitial deletion of chromosome 17 (del(17)(q22q23.3)) confirms a link with oesophageal atresia von MARSH, AIDAN J, WELLESLEY, DIANA, BURGE, DAVID, ASHTON, MARK, BROWNE, CAROLINE E, DENNIS, NICHOLAS R, TEMPLE, I KAREN

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FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosomes 15 and 22: I. Results of 26 new cases von Crolla, John A., Long, Fiona, Rivera, Horacio, Dennis, Nicholas R.

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Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance von Barber, J C, Joyce, C A, Collinson, M N, Nicholson, J C, Willatt, L R, Dyson, H M, Bateman, M S, Green, A J, Yates, J R, Dennis, N R

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Seven ring (X) chromosomes lacking the XIST locus, six with an unexpectedly mild phenotype von TURNER, C, DENNIS, N. R, SKUSE, D. H, JACOBS, P. A

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A study of females with deletions of the short arm of the X chromosome von JAMES, R. S, COPPIN, B, DALTON, P, DENNIS, N. R, MITCHELL, C, SHARP, A. J, SKUSE, D. H, THOMAS, N. S, JACOBS, P. A

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An 11p;17p telomeric translocation in two families associated with recurrent miscarriages andMiller-Dieker syndrome von Joyce, Christine A, Dennis, Nicholas R, Howard, Francis, Davis, Louisa M, Thomas, N Simon

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The fetal valproate syndrome von DiLiberti, John H., Farndon, Peter A., Dennis, Nicholas R., Curry, Cynthia J. R.

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Holoprosencephaly: a family showing dominant inheritance and variable expression von Collins, A L, Lunt, P W, Garrett, C, Dennis, N R

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A molecular and FISH approach to determining karyotype and phenotype correlations in six patients with supernumerary marker(22) chromosomes von Crolla, John A., Howard, Peter, Mitchell, Caroline, Long, Fiona L., Dennis, Nicholas R.

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Characterization of breakpoints in the GABRG3 and TSPY genes in a family with a t(Y;15)(p11.2;q12) von Gole, Leena, Crolla, John A., Thomas, Simon N., Jacobs, Patricia A., Dennis, Nicholas R.

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Lethal syndrome of slender bones, intrauterine fractures, characteristic facial appearance, and cataracts, resembling Hallermann-Streiff syndrome in two sibs von Dennis, Nicholas R., Fairhurst, Joanne, Moore, Isabella E.

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