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2q33
A chromosome band present on 2q
National Institutes of Health
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Related topics
Related topics
9 relations
ABI2 wt Allele
CD28 wt Allele
CTLA4 wt Allele
Chromosomes
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2012
2012
Novel crystallin gamma B mutations in a Kuwaiti family with autosomal dominant congenital cataracts reveal genetic and clinical heterogeneity
S. Alfadhli
,
S. Abdelmoaty
,
Amal Al-Hajeri
,
A. Behbehani
,
F. Alkuraya
Molecular Vision
2012
Corpus ID: 10231836
Purpose To explore the disease locus and causative mutation for autosomal dominant congenital cataracts (ADCC) in a Kuwaiti…
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2009
2009
Novel mutation in the γ-S crystallin gene causing autosomal dominant cataract
V. Vanita
,
J. Singh
,
Daljit Singh
,
R. Varon
,
K. Sperling
Molecular Vision
2009
Corpus ID: 567318
Purpose To identify the underlying genetic defect in a north Indian family with seven members in three-generations affected with…
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2008
2008
Gene Expression Profiles Stratified according to Type 1 Diabetes Mellitus Susceptibility Regions
D. M. Rassi
,
C. Junta
,
+16 authors
E. Donadi
Annals of the New York Academy of Sciences
2008
Corpus ID: 2415037
The MHC region (6p21) aggregates the major genes that contribute to susceptibility to type 1 diabetes (T1D). Three additional…
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Highly Cited
2004
Highly Cited
2004
Genetic association of coeliac disease susceptibility to polymorphisms in the ICOS gene on chromosome 2q33
K. Haimila
,
T. Smedberg
,
+4 authors
P. Holopainen
Genes and Immunity
2004
Corpus ID: 22120082
An interesting candidate gene region for coeliac disease (CD), a common multifactorial disease, is a segment on 2q33–37…
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Review
2003
Review
2003
A female infant with duplication of chromosome 2q33 to 2q37.3
A. Slavotinek
,
Debra Boles
,
F. Lacbawan
Clinical Dysmorphology
2003
Corpus ID: 45833689
We report a 13-month-old female child with a de-novo inverted duplication of chromosome 2q extending from 2q33 to 2q37.3. She had…
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2003
2003
No Association of CTLA4 Gene With Celiac Disease in the Basque Population
A. Martín-Pagola
,
G. D. de Nanclares
,
+4 authors
L. Castaño
Journal of Pediatric Gastroenterology and…
2003
Corpus ID: 35513218
Background Celiac disease (CD) is an autoimmune disorder caused by intolerance to ingested gluten that develops in genetically…
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2001
2001
The DIRC1 gene at chromosome 2q33 spans a familial RCC-associated t(2;3)(q33;q21) chromosome translocation
T. Druck
,
J. Podolski
,
+6 authors
K. Huebner
Journal of Human Genetics
2001
Corpus ID: 19436285
AbstractA reciprocal, balanced, constitutional chromosome translocation, t(2;3)(q33;q21), which is associated with familial clear…
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Highly Cited
2001
Highly Cited
2001
Allergic rhinitis – a total genome-scan for susceptibility genes suggests a locus on chromosome 4q24-q27
A. Haagerup
,
T. Bjerke
,
P. O. Schøitz
,
H. Binderup
,
R. Dahl
,
T. Kruse
European Journal of Human Genetics
2001
Corpus ID: 21921258
Allergic rhinitis is a common disease of complex inheritance and is characterised by mucosal inflammation caused by allergen…
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1990
1990
Assignment of the human nicotinic acetylcholine receptor genes: the alpha and delta subunit genes to chromosome 2 and the beta subunit gene to chromosome 17
D. Beeson
,
S. Jeremiah
,
L. West
,
S. Povey
,
J. Newsom-Davis*
Annals of Human Genetics
1990
Corpus ID: 151624
The chromosomal assignments of the genes coding for the alpha, beta and delta subunits of the human nicotinic acetylcholine…
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1978
1978
Duplication 2q33 leads to 2q37 due to paternal ins (12;2) translocation.
N. Dennis
,
R. Neu
,
R. Bannerman
American journal of medical genetics
1978
Corpus ID: 37555751
An 18 month-old boy with partial duplication of the long arm of chromosome 2, based on a paternal balanced translocation, 46,XY…
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