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FRA16B gene
Known as:
FRA16B
, fragile site, distamycin A type, rare, fra(16)(q22.1)
National Institutes of Health
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Related topics
Related topics
1 relation
FRA10A gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Enhanced Expression of FRA16B using AT-Rich DNA Binding Chemicals in a Woman with Secondary Amenorrhoea.
G. Bhavani
,
S. Sivaprakash
,
Chandra R. Samuel
,
S. Santhiya
Journal of clinical and diagnostic research…
2017
Corpus ID: 43109012
Fragile sites represent regions of chromatin that fail to compact during mitosis. Based on the prevalence and pattern of…
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2012
2012
Spontaneous expression of FRA16B in a non‐consanguineous couple experiencing multiple fetal losses
S. Aswini
,
T. Jegatheesan
,
N. Chandra
The journal of obstetrics and gynaecology…
2012
Corpus ID: 21470865
The association between fragile sites and human genetic diseases is still debatable. Although FRAXA and FRAXE have been found to…
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2004
2004
Homozygotes for FRA16B are Normal
Trudy Hocking
,
W. Feichtinger
,
M. Schmid
,
E. Haan
,
E. Baker
,
G. Sutherland
Chromosome Research
2004
Corpus ID: 33811591
Homozygotes for the rare folate-sensitive autosomal fragile sites have never been recorded. Two non-folate-sensitive rare fragile…
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2000
2000
A novel minisatellite repeat expansion identified at FRA16B in a Japanese carrier.
M. Yamauchi
,
S. Tsuji
,
K. Mita
,
T. Saito
,
M. Morimyo
Genes & Genetic Systems
2000
Corpus ID: 22870721
Previously, the allelic expansion of a 33-bp AT-rich minisatellite repeat has been reported to cause FRA16B, a distamycin A…
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2000
2000
Spectral karyotyping of Werner syndrome fibroblast cultures
Ralph E. Melcher
,
R. V. Golitschek
,
+5 authors
H. Hoehn
Cytogenetic and Genome Research
2000
Corpus ID: 32955295
Fibroblast cultures from two Werner syndrome patients were analyzed by spectral karyotyping. There were multiple, pseudodiploid…
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1998
1998
Molecular analysis of FRA16B at 16q22.1 in Japanese population.
M. Yamauchi
,
N. Seki
,
+4 authors
T. Hori
1998
Corpus ID: 83129696
1991
1991
“Spontaneous” FRA16B is a hot spot for sister chromatid exchanges
T. Lukusa
,
Ernest Meulepas
,
J. Fryns
,
H. Berghe
,
J. Cassiman
Human Genetics
1991
Corpus ID: 26781872
SummarySix heterozygous carriers of a fragile site at 16q22 were available for the current study. We demonstrated that the…
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1990
1990
Differential expression of FRA16B in peripheral lymphocytes and bone marrow cells.
M. Zollino
,
M. Genuardi
,
G. Neri
Cancer Genetics and Cytogenetics
1990
Corpus ID: 35107356
1989
1989
A linkage group with FRA16B (the fragile site at 16q22.1)
J. Mulley
,
V. Hyland
,
A. Fratini
,
L. Bates
,
A. Gedeon
,
G. Sutherland
Human Genetics
1989
Corpus ID: 26890471
SummaryPolymorphic DNA markers located in bands 16q13, 16q21 and 16q22 were examined for recombination with FRA16B, the fragile…
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1988
1988
Fine mapping of gene probes and anonymous DNA fragments to the long arm of chromosome 16.
D. Callen
,
V. Hyland
,
+4 authors
G. Sutherland
Genomics
1988
Corpus ID: 28442525
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