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Examining the family-centred approach to genetic testing and counselling among UK Pakistanis: a community perspective.
J Community Genet. 2013 Jan;4(1):49-57. doi: 10.1007/s12687-012-0117-x. Epub 2012 Oct 21.
J Community Genet. 2013.
PMID: 23086468
Free PMC article.
Addressing key issues in the consanguinity-related risk of autosomal recessive disorders in consanguineous communities: lessons from a qualitative study of British Pakistanis.
J Community Genet. 2016 Jan;7(1):65-79. doi: 10.1007/s12687-015-0252-2. Epub 2015 Sep 12.
J Community Genet. 2016.
PMID: 26363620
Free PMC article.
Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phenotypic variation.
J Med Genet. 2002 Oct;39(10):718-21. doi: 10.1136/jmg.39.10.718.
J Med Genet. 2002.
PMID: 12362027
Free PMC article.
A gene for ataxic cerebral palsy maps to chromosome 9p12-q12.
Eur J Hum Genet. 2000 Apr;8(4):267-72. doi: 10.1038/sj.ejhg.5200445.
Eur J Hum Genet. 2000.
PMID: 10854109
Protein-truncating mutations in ASPM cause variable reduction in brain size.
Am J Hum Genet. 2003 Nov;73(5):1170-7. doi: 10.1086/379085. Epub 2003 Oct 21.
Am J Hum Genet. 2003.
PMID: 14574646
Free PMC article.
Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter.
Am J Hum Genet. 1998 Aug;63(2):541-6. doi: 10.1086/301966.
Am J Hum Genet. 1998.
PMID: 9683597
Free PMC article.
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