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4q21
A chromosome band present on 4q
National Institutes of Health
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Related topics
Related topics
13 relations
AFF1 wt Allele
CXCL1 wt Allele
CXCL10 wt Allele
CXCL13 wt Allele
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Papers overview
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Review
2017
Review
2017
Amelogenesis Imperfecta in Children: Review of Pathogenetic Aspect
H. Achmad
,
Hasanuddin Thahir
,
Mardiana A. Adam
2017
Corpus ID: 43107285
Amelogenesis imperfecta is an abnormal formation of the enamel. This anomaly associated with malformation of proteins, such as…
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2014
2014
Exon Sequencing of PKD 1 Gene in an Iranian Patient with Autosomal-Dominant Polycystic Kidney Disease
Atousa Hafizi
,
S. Khatami
,
H. Galehdari
,
G. Shariati
,
A. Saberi
,
M. Hamid
2014
Corpus ID: 38705648
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common genetic kidney disorders with the…
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Review
2012
Review
2012
Angiogenesis and the Pathogenesis of Autosomal Dominant Polycystic Kidney Disease
B. Reed
,
Wei Wang
2012
Corpus ID: 53456743
Occurring with an incidence between 1/400 – 1/1000 live births autosomal dominant polycystic kidney disease (ADPKD) is the most…
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2008
2008
Breakprone chromosome bands in lymphocytes from sarcoma patients do not coincide with bands involved in primary sarcoma-associated chromosome rearrangements.
F. Mertens
,
B. Johansson
Hereditas
2008
Corpus ID: 27311147
The localization of breakpoints in spontaneous chromosome aberrations, i.e., chromatid and chromosome gaps, breaks, and exchanges…
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2004
2004
Amelogenesis Imperfecta in a New Animal Model—a Mutation in Chromosome 5 (human 4q21)
H. Seedorf
,
I. Springer
,
+5 authors
Y. Açil
Journal of dentistry research
2004
Corpus ID: 23591671
Candidate genes for amelogenesis imperfecta (AI) and dentinogenesis imperfecta (DI) are located on 4q21 in humans. We tested our…
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2003
2003
The Chromosome 4 q 21 Gene ( AF-4 / FEL ) Is Widely Expressed in Normal Tissues and Shows Breakpoint Diversity in t ( 4 ; 1 l ) ( q 21 ; q 23 ) Acute Leukemia
C. Chen
,
J. Hilden
,
+6 authors
Kersey
2003
Corpus ID: 30144998
The chromosomal translocation, t (4 ; l l )(q21 ;q23), is the most common type of 1 1 q23 chromosomal abnormality, being highly…
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2002
2002
Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers.
Wei-De Lin
,
Jer-Yuarn Wu
,
F. Tsai
,
M. Gau
,
Cheng-Chung Lee
Journal of the Formosan Medical Association…
2002
Corpus ID: 27372646
Autosomal dominant polycystic kidney disease (ADPKD), is an inherited disorder with genetic heterogeneity. The presence of renal…
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2002
2002
Hyper-IgE-syndrome
E. D. Renner
,
B. H. Belohradsky
,
B. Grimbacher
2002
Corpus ID: 79404595
The hyper-IgE syndrome (HIES) is a rare primary immunodeficiency, characterized by eczema, elevated total IgE, and recurrent…
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2002
2002
Klinisch-genetische Definition des Hyper-IgE-Syndroms (HIES)
E. Renner
2002
Corpus ID: 70562763
Das Hyper-IgE-Syndrom (HIES) ist ein seltener primarer Immundefekt, charakterisiert durch die klinische Trias: chronisches Ekzem…
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1999
1999
Initial genome wide parametric genetic linkage analysis of schizophrenia and schizophrenia spectrum disorders finds lod scores above 3.00 on four chromosomes at 1Q22-23, 5Q22-35, 8P21-23 and 11Q14-24…
H. Gurling
,
G. Kalsi
,
+8 authors
D. Curtis
1999
Corpus ID: 70650325