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3q21-q24
A chromosome band present on 3q
National Institutes of Health
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Chromosomes
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Rhodopsin p.N78I dominant mutation causing sectorial retinitis pigmentosa in a pedigree with intrafamilial clinical heterogeneity.
David Rivera-de la Parra
,
Jesús Cabral-Macías
,
M. Matías-Florentino
,
Gabriela Rodríguez-Ruiz
,
V. Robredo
,
J. Zenteno
Gene
2013
Corpus ID: 205015534
Review
2007
Review
2007
A review on Hailey-Hailey disease
T. Cheng
2007
Corpus ID: 40100035
Hailey-Hailey disease (HHD) is a rare autosomal dominant blistering skin disease first described in 1939. It is characterised by…
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2006
2006
A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5 q
C. Pang
,
B. Fan
,
+7 authors
R. Ritch
2006
Corpus ID: 45051917
Glaucoma is a leading cause of vision impairment and blindness in both developed and developing countries. Primary open angle…
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2004
2004
Exclusion of 14 candidate loci for primary open angle glaucoma in Finnish families.
S. Lemmelä
,
T. Ylisaukko‐oja
,
E. Forsman
,
I. Järvelä
Molecular Vision
2004
Corpus ID: 2567249
PURPOSE The aim of the present study was to examine the genetic background of primary open angle glaucoma (POAG) in the Finnish…
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1994
1994
No uniparental disomy for chromosome 3 in Brachmann-De Lange syndrome.
N. De Marchi
,
S. Antonarakis
,
L. Jackson
American journal of medical genetics
1994
Corpus ID: 27249614
Brachmann-De Lange syndrome (BDLS, MIM No. 122470) is a well-described genetic syndrome of mental retardation and multiple…
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