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4q12
A chromosome band present on 4q
National Institutes of Health
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5 relations
CLOCK wt Allele
Chromosomes
FIP1L1 wt Allele
IGFBP7 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Integrative analysis of copy number alteration and gene expression profiling in ovarian clear cell adenocarcinoma.
C. Sung
,
C. Choi
,
+11 authors
Byoung-Gie Kim
Cancer Genetics
2013
Corpus ID: 22281805
2008
2008
High-resolution array comparative genomic hybridization analysis of human bronchial and salivary adenoid cystic carcinoma
A. Bernheim
,
S. Toujani
,
+7 authors
P. Fouret
Laboratory Investigation
2008
Corpus ID: 15365875
Adenoid cystic carcinoma (ACC) is a rare but distinctive tumor. Oligonucleotide array comparative genomic hybridization has been…
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2008
2008
A locus for autosomal dominant progressive non‐syndromic hearing loss, DFNA27, is on chromosome 4q12‐13.1
LM Peters
,
R. Fridell
,
+5 authors
R. Morell
Clinical Genetics
2008
Corpus ID: 205406598
We ascertained a large North American family, LMG2, segregating progressive, non‐syndromic, sensorineural hearing loss. A genome…
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Highly Cited
2005
Highly Cited
2005
Molecular characterization of the idiopathic hypereosinophilic syndrome (HES) in 35 French patients with normal conventional cytogenetics
C. Roche-Lestienne
,
S. Lepers
,
+22 authors
and The French Eosinophil Network
Leukemia
2005
Corpus ID: 12176392
Idiopathic hypereosinophilic syndrome (HES) characterized by unexplained and persistent hypereosinophilia is heterogeneous and…
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Highly Cited
2005
Highly Cited
2005
The hypereosinophilic syndrome: fluorescence in situ hybridization detects the del(4)(q12)-FIP1L1/PDGFRA but not genomic rearrangements of other tyrosine kinases.
R. la Starza
,
G. Specchia
,
+11 authors
C. Mecucci
Haematologica
2005
Corpus ID: 24314808
BACKGROUND AND OBJECTIVES According to WHO criteria, the idiopathic hypereosinophilic syndrome (HES) is defined as persistent…
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Review
2004
Review
2004
Imatinib therapy for hypereosinophilic syndrome and eosinophilia-associated myeloproliferative disorders.
A. Pardanani
,
A. Tefferi
Leukemia research : a Forum for Studies on…
2004
Corpus ID: 30478832
2001
2001
Analysis of genetic changes in rat endometrial carcinomas by means of comparative genomic hybridization.
K. Helou
,
A. Walentinsson
,
+5 authors
G. Levan
Cancer Genetics and Cytogenetics
2001
Corpus ID: 6651938
1995
1995
Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4.
Y. Y. Fang
,
H. Eyre
,
+5 authors
D. Callen
American Journal of Human Genetics
1995
Corpus ID: 23628824
Molecular cloning of a microdissected small accessary ring chromosome 4 from a moderately retarded and dysmorphic patient has…
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1994
1994
Assignment of the true and processed genes for human glycine decarboxylase to 9p23-24 and 4q12.
M. Isobe
,
H. Koyata
,
T. Sakakibara
,
K. Momoi-Isobe
,
K. Hiraga
Biochemical and Biophysical Research…
1994
Corpus ID: 46047467
Southern analysis using a human glycine decarboxylase cDNA probe and genomic DNA preparations from Chinese hamster-human…
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1986
1986
Tentative assignment of piebald trait gene to chromosome band 4q12
J. Hoo
,
R. Haslam
,
C. Orman
Human Genetics
1986
Corpus ID: 42728569
SummaryA case of de novo del(4)(q12q21.1) is presented. Three of four patients with comparable deletion show abnormal…
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