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4p16.3
A chromosome band present on 4p
National Institutes of Health
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Related topics
Related topics
9 relations
Chromosome 4 Short Arm
Chromosomes
FGFR3 wt Allele
HTT wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Wolf-Hirschhorn Syndrome with Buphthalmos
Rugmini Kamalammal
,
L. Subha
,
S. Rao
2014
Corpus ID: 54038323
Wolf-Hirschhorn syndrome is a 4p-deletion syndrome in which there is reduced growth, abnormal phenotype, developmental delay…
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Review
2011
Review
2011
WHSC1 (Wolf-Hirschhorn syndrome candidate 1)
Eva Martínez-García
,
Jonathan D. Licht
2011
Corpus ID: 84303390
Review on WHSC1 (Wolf-Hirschhorn syndrome candidate 1), with data on DNA, on the protein encoded, and where the gene is…
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2006
2006
Integrative Analysis of NCI-60 Panel Reveals Candidate Key Genetic Regulators Affected by Genomic Alterations
D. Lipson
,
M. Reimers
,
+6 authors
Z. Yakhini
2006
Corpus ID: 14348771
The NCI-60 panel [1], which consists of 60 human cancer cell lines derived from 9 different tissues of origin, has been…
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2001
2001
The Gene for Cherubism Maps to Chromosome
J. Mangion
,
N. Rahman
,
+7 authors
M. Stratton
2001
Corpus ID: 39468779
Cherubism is a rare familial disease of childhood characterized by proliferative lesions within the mandible and maxilla that…
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2001
2001
Characterization of the t(4;14)(p16.3;q32) in the KMS-18 multiple myeloma cell line
Domenica Ronchetti
,
Silvia Bogni
,
+4 authors
A. Neri
Leukemia
2001
Corpus ID: 26663071
Chromosomal translocations involving the immunoglobulin heavy chain (IGH) locus at chromosome 14q32 represent a frequent event in…
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2001
2001
Genotype-phenotype correlations in Wolf-Hirschhorn syndrome.
M. Zollino
,
G. Neri
European Journal of Human Genetics
2001
Corpus ID: 195690449
In a recent issue of the journal, Wieczorek et al. reported on a clinical, cytogenetic and molecular analysis of 13…
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2001
2001
Choroid plexus cysts and oligohydramnios: presenting echographic signs in a female fetus with deletion of the Wolf-Hirschhorn syndrome region (4p16.3).
I. Witters
,
D. Van Schoubroeck
,
J. Fryns
Genetic Counseling
2001
Corpus ID: 12675558
2001
2001
associated with chromosome 13 abnormalities in both multiple myeloma and monoclonal gammopathy of undetermined significance
Van Wier
,
R. J. Bailey
,
+15 authors
Wm.
2001
Corpus ID: 6331052
We read with great interest the paper by Chesi et al regarding FGFR3that further supports the role of FGFR3in the pathogenesis of…
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2000
2000
Advances in Brief Detection of t ( 4 ; 14 ) ( p 16 . 3 ; q 32 ) Chromosomal Translocation in Multiple Myeloma by Reverse Transcription-Polymerase Chain Reaction Analysis of IGH-MMSET Fusion…
Ursula Malgeri
,
L. Baldini
,
+9 authors
A. Neri
2000
Corpus ID: 36270966
We and others have recently identified a novel recurring t(4;14)(p16.3; q32) translocation in multiple myeloma (MM) that leads to…
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Highly Cited
1992
Highly Cited
1992
Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndrome.
R. Tupler
,
L. Bortotto
,
+5 authors
P. Maraschio
Journal of Medical Genetics
1992
Corpus ID: 35875136
The parental origin of the de novo deleted chromosome 4 was studied in five cases of Wolf-Hirschhorn syndrome using polymorphic…
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