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2q35-q37
A chromosome band present on 2q
National Institutes of Health
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Related topics
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2 relations
Chromosomes
PAX3 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Molecular cytogenetic characterization of a 2q35‐q37 duplication and a 4q35.1‐q35.2 deletion in two cousins: A genotype–phenotype analysis
L. Ronzoni
,
A. Peron
,
+5 authors
M. Bedeschi
American Journal of Medical Genetics. Part A
2015
Corpus ID: 25471878
The 2q3 duplication and 4q3 deletion are two distinct conditions with variable phenotypes including developmental delay…
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Highly Cited
2001
Highly Cited
2001
Identification of a new mutation in the alpha4(IV) collagen gene in a family with autosomal dominant Alport syndrome and hypercholesterolaemia.
M. Ciccarese
,
D. Casu
,
+5 authors
A. Satta
Nephrology, Dialysis and Transplantation
2001
Corpus ID: 42513211
BACKGROUND Alport syndrome (AS) is a hereditary disease of the glomerular basement membrane in the kidney characterized by…
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2000
2000
A locus for brachydactyly type A-1 maps to chromosome 2q35-q36.
Xinping Yang
,
Chaowen She
,
+6 authors
Lin He
American Journal of Human Genetics
2000
Corpus ID: 30703820
Brachydactyly type A-1 (BDA1) was, in 1903, the first recorded example of a human anomaly with Mendelian autosomal dominant…
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Highly Cited
2000
Highly Cited
2000
Patterns of chromosomal imbalances in invasive breast cancer
F. Richard
,
M. Pacyna‐Gengelbach
,
+6 authors
A. Schwendel
International Journal of Cancer
2000
Corpus ID: 25605556
Invasive breast carcinomas are characterized by a complex pattern of chromosomal alterations. We applied comparative genomic…
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Review
2000
Review
2000
Trisomy 1q, 2, and 20 in a case of hepatoblastoma: possible significance of 2q35-q37 and 1q12-q21 rearrangements.
Y. A. Yeh
,
P. Rao
,
C. T. Cigna
,
W. Middlesworth
,
J. Lefkowitch
,
V. Murty
Cancer Genetics and Cytogenetics
2000
Corpus ID: 42676124
Review
1999
Review
1999
Trisomy 2q35-q37 due to insertion of 2q material into 17q25: clinical, cytogenetic, and molecular cytogenetic characterization.
B. Fritz
,
J. Müller‐Navia
,
Ulrike Hillig
,
Martin Köhler
,
M. Aslan
,
Helga Rehder
American journal of medical genetics
1999
Corpus ID: 20345039
We present a 7-year-old boy with growth retardation, developmental and mental delay, and minor physical abnormalities. The…
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1995
1995
Assignment of the human glypican gene (GPC1) to 2q35-q37 by fluorescence in situ hybridization.
J. Vermeesch
,
Griet Mertens
,
Guido David
,
P. Marynen
Genomics
1995
Corpus ID: 11036076
Highly Cited
1993
Highly Cited
1993
An RFLP map for 2q33‐q37 from multicase mycobacterial and leishmanial disease families: no evidence for an Lsh/Ity/Bcg gene homologue influencing susceptibility to leprosy
Marie-Anne Shaw
,
Shannon Atkinson
,
+10 authors
Jenefer M. Blackwell
Annals of Human Genetics
1993
Corpus ID: 36232886
The mycobacterial disease leprosy and tuberculosis (TB) and the leishmaniases are characterized by a wide spectrum of disease…
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1992
1992
Construction and characterization of a region-specific microdissection library from human chromosome 2q35-q37.
Jingwei Yu
,
S. Tong
,
Teresa Yang-Feng
,
F. Kao
,
F. Kao
Genomics
1992
Corpus ID: 39208279
Review
1991
Review
1991
Cytogenetic Studies in Acute Promyelocytic Leukemia: A Survey of Secondary Chromosomal Abnormalities
R. Berger
,
M. Coniat
,
J. Derré
,
D. Vecchione
,
P. Jonveaux
Genes, Chromosomes and Cancer
1991
Corpus ID: 33490599
A series of 105 patients with acute promyelocytic leukemia (APL) has been cytogenetically investigated at the Department of…
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