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5q33-q35
A chromosome band present on 5q
National Institutes of Health
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Related topics
Related topics
4 relations
CSF1R wt Allele
Chromosomes
Oncogene CSF1R
chromosome 5q
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2003
2003
Genome Scan of Two Large Families with Adult-Onset Primary Open Angle Glaucoma (POAG) Suggests a Probable Locus on 5q33-q35
S. Monemi
,
A. Child
,
O. Lehmann
,
G. Spaeth
,
R. Crick
,
M. Sarfarazi
2003
Corpus ID: 82129800
Highly Cited
1999
Highly Cited
1999
A genome-wide search identifies potential new susceptibility loci for Crohn's disease.
Yuanhong Ma
,
Jeffrey D. Ohmen
,
+7 authors
Huiying Yang
Inflammatory Bowel Diseases
1999
Corpus ID: 24346708
Chronic inflammatory bowel disease (IBD) presents as two major clinical forms, Crohn's disease (CD) and ulcerative colitis (UC…
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1999
1999
Pure partial trisomy 5q33-->5q35 resulting from the adjacent-1 segregation of a paternal (5;14)(q33;p12) translocation.
A. Paoloni-Giacobino
,
A. Bottani
,
S. Dahoun
Annales de Genetique
1999
Corpus ID: 40531338
A 14-year-old male was referred for evaluation of mental retardation with short stature and dysmorphic features. His karyotype…
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1997
1997
Hyperekplexia-like syndromes without mutations in the GLRA1 gene
M. Vergouwe
,
M. Tijssen
,
+4 authors
R. Frants
Clinical neurology and neurosurgery (Dutch…
1997
Corpus ID: 43274005
1996
1996
Co‐dominant Inheritance of Hyperekplexia and Spastic Paraparesis
P. Baxter
,
S. Connolly
,
+4 authors
D. Gardner‐medwin
Developmental Medicine & Child Neurology
1996
Corpus ID: 8218833
In four generations of a family with autosomal dominant hyperekplexia (startle disease), untreated affected adult members had pes…
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Review
1996
Review
1996
[Familial hyperekplexia: startle disease. Clinical, electrophysiological and genetic study of a family].
A. Bernasconi
,
F. Regli
,
Schorderet Df
,
G. Pescia
Revue neurologique (Paris)
1996
Corpus ID: 24907356
The major form of familial hyperekplexia, a rare autosomal dominant disorder, is characterized by an abnormal startle reaction…
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Highly Cited
1992
Highly Cited
1992
Startle disease, or hyperekplexia: Response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis
S. Ryan
,
S. Sherman
,
J. Terry
,
R. Sparkes
,
M. Torres
,
Ray W. Mackey
Annals of Neurology
1992
Corpus ID: 28879043
Familial startle disease (also known as hyperekplexia and congenital “stiff‐man” syndrome) is an autosomal dominant disorder…
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1992
1992
Sublocalization of the chromosome 5 breakpoint of the 3;5 translocation in myelodysplastic syndromes and acute myeloid leukemia.
S. Morris
,
J. T. Foust
,
M. Valentine
,
W. Roberts
,
D. Shapiro
,
A. Look
Genes, Chromosomes and Cancer
1992
Corpus ID: 39862827
A t(3;5)(q25.1;q34) reciprocal translocation identifies a subset of cases of myelodysplastic syndrome or acute myeloid leukemia…
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