Everett, KV; Chioza, BA; Georgoula, C; Reece, A; Capon, F; Parker, KA; Cord-Udy, C; McKeigue, P; Mitton, S; Pierro, A; et al. Everett, KV; Chioza, BA; Georgoula, C; Reece, A; Capon, F; Parker, KA; Cord-Udy, C; McKeigue, P; Mitton, S; Pierro, A; Puri, P; Mitchison, HM; Chung, EM; Gardiner, RM (2008) Genome-wide high-density SNP-based linkage analysis of infantile hypertrophic pyloric stenosis identifies loci on chromosomes 11ql4-q22 and xq23. AMERICAN JOURNAL OF HUMAN GENETICS, 82 (3). 756 - 762 (7). ISSN 0002-9297 https://doi.org/10.1016/j.ajhg.2007.12.023
SGUL Authors: Chioza, Barry Andrew Mitton, Sally Gay Everett, Kate Victoria

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Item Type:	Article
Additional Information:	PubMed ID: 18308288
Keywords:	Chromosome Mapping, Chromosomes, Human, Pair 11, Female, Genetic Linkage, Genetic Predisposition to Disease, Genome, Human, Humans, Infant, Male, Pedigree, Polymorphism, Single Nucleotide, Pyloric Stenosis, Hypertrophic, Sex Ratio, Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, NITRIC-OXIDE SYNTHASE, RECEPTOR POTENTIAL SUPERFAMILY, SMOOTH-MUSCLE-CELLS, CATION CHANNEL, COMPLEX TRAITS, ERYTHROMYCIN, GENE, EPIDEMIOLOGY, TRPC6, ACTIVATION
SGUL Research Institute / Research Centre:	Academic Structure > Institute of Medical & Biomedical Education (IMBE) Academic Structure > Institute of Medical & Biomedical Education (IMBE) > Centre for Biomedical Education (INMEBE) Academic Structure > Institute of Medical & Biomedical Education (IMBE) > Centre for Clinical Education (INMECE )
Journal or Publication Title:	AMERICAN JOURNAL OF HUMAN GENETICS
ISSN:	0002-9297
Related URLs:	Author
Dates:	Date Event 1 March 2008 Published
Web of Science ID:	WOS:000254067800020
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URI:	https://openaccess.sgul.ac.uk/id/eprint/2140
Publisher's version:	https://doi.org/10.1016/j.ajhg.2007.12.023

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