Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from Pakistan

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Publication year
2013Source
Clinical Genetics, 84, 3, (2013), pp. 290-3ISSN
Publication type
Article / Letter to editor

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Organization
Human Genetics
Ophthalmology
CMBI
Journal title
Clinical Genetics
Volume
vol. 84
Issue
iss. 3
Page start
p. 290
Page end
p. 3
Subject
NCMLS 6: Genetics and epigenetic pathways of disease; NCMLS 6: Genetics and epigenetic pathways of disease IGMD 3: Genomic disorders and inherited multi-system disorders; NCMLS 7: Chemical and physical biologyThis item appears in the following Collection(s)
- Academic publications [227695]
- Electronic publications [108794]
- Faculty of Medical Sciences [87091]
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