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	1.	Estimate of the prevalence of chromosome 15q11-q13 duplications. [electronic resource] by Thomas, N Simon Roberts, S E Browne, C E Producer: 20040324 In: American journal of medical genetics. Part A vol. 120A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	The distinguishing sequence characteristics of mouse imprinted genes. [electronic resource] by Ke, Xiayi Thomas, N Simon Robinson, David O Collins, Andrew Producer: 20030520 In: Mammalian genome : official journal of the International Mammalian Genome Society vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel approach for identifying candidate imprinted genes through sequence analysis of imprinted and control genes. [electronic resource] by Ke, Xiayi Thomas, N Simon Robinson, David O Collins, Andrew Producer: 20030122 In: Human genetics vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Diagnostic screening identifies a wide range of mutations involving the SHOX gene, including a common 47.5 kb deletion 160 kb downstream with a variable phenotypic effect. [electronic resource] by Bunyan, David J Baker, Kevin R Harvey, John F Thomas, N Simon Producer: 20160415 In: American journal of medical genetics. Part A vol. 161A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	SHOX mutations in a family and a fetus with Langer mesomelic dwarfism. [electronic resource] by Thomas, N Simon Maloney, Viv Bass, Paul Mulik, Varsha Wellesley, Diana Castle, Bruce Producer: 20050112 In: American journal of medical genetics. Part A vol. 128A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Investigation of the origins of human autosomal inversions. [electronic resource] by Thomas, N Simon Bryant, Victoria Maloney, Vivienne Cockwell, Annette E Jacobs, Patricia A Producer: 20080624 In: Human genetics vol. 123 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	An 11p;17p telomeric translocation in two families associated with recurrent miscarriages and Miller-Dieker syndrome. [electronic resource] by Joyce, Christine A Dennis, Nicholas R Howard, Francis Davis, Louisa M Thomas, N Simon Producer: 20030610 In: European journal of human genetics : EJHG vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	De novo deletions and duplications detected by array CGH: a study of parental origin in relation to mechanisms of formation and size of imbalance. [electronic resource] by Sibbons, Charlene Morris, Joan K Crolla, John A Jacobs, Patricia A Thomas, N Simon Producer: 20120507 In: European journal of human genetics : EJHG vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A de novo duplication of Xp11.22-p11.4 in a girl with intellectual disability, structural brain anomalies, and preferential inactivation of the normal X chromosome. [electronic resource] by Holden, Simon T Clarkson, Amanda Thomas, N Simon Abbott, Kristin James, Matthew R Willatt, Lionel Producer: 20100929 In: American journal of medical genetics. Part A vol. 152A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Breakpoint mapping and haplotype analysis of three reciprocal translocations identify a novel recurrent translocation in two unrelated families: t(4;11)(p16.2;p15.4). [electronic resource] by Thomas, N Simon Maloney, Viv Bryant, Victoria Huang, Shuwen Brewer, Carole Lachlan, Katherine Jacobs, Patricia A Producer: 20090326 In: Human genetics vol. 125 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	De novo apparently balanced translocations in man are predominantly paternal in origin and associated with a significant increase in paternal age. [electronic resource] by Thomas, N Simon Morris, Joan K Baptista, Julia Ng, Bee Ling Crolla, John A Jacobs, Patricia A Producer: 20100506 In: Journal of medical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Duplications of chromosome 11p15 of maternal origin result in a phenotype that includes growth retardation. [electronic resource] by Fisher, Andrew M Thomas, N Simon Cockwell, Annette Stecko, Olga Kerr, Bronwyn Temple, I Karen Clayton, Peter Producer: 20021202 In: Human genetics vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Detailed clinical and molecular study of 20 females with Xq deletions with special reference to menstruation and fertility. [electronic resource] by Mercer, Catherine L Lachlan, Katherine Karcanias, Alexandra Affara, Nabeel Huang, Shuwen Jacobs, Patricia A Thomas, N Simon Producer: 20130611 In: European journal of medical genetics vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Transmitted duplication of 12q21.32-12q22 includes 48 genes and has no apparent phenotypic consequences. [electronic resource] by Barber, John C K Maloney, Viv K Kirchhoff, Maria Thomas, N Simon Boyle, Tracy A Castle, Bruce Producer: 20070508 In: American journal of medical genetics. Part A vol. 143A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Parental and chromosomal origin of unbalanced de novo structural chromosome abnormalities in man. [electronic resource] by Thomas, N Simon Durkie, Miranda Van Zyl, Berendine Sanford, Richard Potts, Gemma Youings, Sheila Dennis, Nicholas Jacobs, Patricia Producer: 20060912 In: Human genetics vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Prader-Willi syndrome--a study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders. [electronic resource] by Veltman, Marijcke W M Thompson, Russell J Roberts, Sian E Thomas, N Simon Whittington, Joyce Bolton, Patrick F Producer: 20040527 In: European child & adolescent psychiatry vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Large de novo deletion of 7p15.1 to 7p12.1 involving the imprinted gene GRB10 associated with a complex phenotype including features of Beckwith Wiedemann syndrome. [electronic resource] by Naik, Swati Riordan-Eva, Elliott Thomas, N Simon Poole, Rebecca Ashton, Mark Crolla, John A Temple, I Karen Producer: 20110614 In: European journal of medical genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Functional disomy resulting from duplications of distal Xq in four unrelated patients. [electronic resource] by Lachlan, Katherine L Collinson, Morag N Sandford, Richard O C van Zyl, Berendine Jacobs, Patricia A Thomas, N Simon Producer: 20041116 In: Human genetics vol. 115 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Parental and chromosomal origins of microdeletion and duplication syndromes involving 7q11.23, 15q11-q13 and 22q11. [electronic resource] by Thomas, N Simon Durkie, Miranda Potts, Gemma Sandford, Richard Van Zyl, Berendine Youings, Sheila Dennis, Nicholas R Jacobs, Patricia A Producer: 20060822 In: European journal of human genetics : EJHG vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	DNA methylation profiling in X;autosome translocations supports a role for L1 repeats in the spread of X chromosome inactivation. [electronic resource] by Bala Tannan, Neeta Brahmachary, Manisha Garg, Paras Borel, Christelle Alnefaie, Randah Watson, Corey T Thomas, N Simon Sharp, Andrew J Producer: 20141015 In: Human molecular genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 37 results.