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10q25
A chromosome band present on 10q
National Institutes of Health
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Related topics
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6 relations
10q
CASP7 wt Allele
Chromosomes
DUSP5 wt Allele
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2012
2012
Further contributions towards the molecular analysis of NIPBL and SMC1A genes in a cohort of patients with Cornelia de Lange Syndrome
Eurico Costa
2012
Corpus ID: 145092266
Dissertacao de Mestrado em Biologia apresentada a Faculdade de Ciencias da Universidade do Porto, 2012
2001
2001
Prostatic expression of hensin, a protein implicated in epithelial terminal differentiation
Jian Ma
,
J. Takito
,
Srinivasan Vijayakumar
,
D. Peehl
,
C. Olsson
,
Q. Al-Awqati
The Prostate
2001
Corpus ID: 33550624
Hensin induces terminal differentiation in rabbit kidney collecting tubule cells. Rabbit hensin and human DMBT1 result from…
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1986
1986
A fragile site 10q25 in human sperm chromosomes.
R. Martín
Journal of Medical Genetics
1986
Corpus ID: 1875196
During a study of sperm chromosomal abnormalities in normal men,' 2we found a donor who expressed the fragile site at 10q25 in…
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1985
1985
Enhanced expression of chromosome fragile site 10q25 in chronic myelogenous leukemia.
Rodman Morgan
,
Stephanie S. Morgan
,
Frederick Hecht
,
John M. Opitz
,
James F. Reynolds
American journal of medical genetics
1985
Corpus ID: 46084448
Spontaneous expression of a BrdU-sensitive fragile site at 10q25 was observed in normal lymphocytes and malignant blood and bone…
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1984
1984
[Autosomal fragile sites].
M. Jotterand-Bellomo
Journal de genetique humaine
1984
Corpus ID: 43673914
It is possible to distribute the 17 autosomic fragile sites presently known in three categories according to their sensitivity…
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1983
1983
Spontaneous expression of the chromosome fragile site fra(10)(q25).
A. M. Taylor
,
S. Bundey
American Journal of Human Genetics
1983
Corpus ID: 45507172
We report the spontaneous expression of the chromosome fragile site at 10q25 in a child with progressive cerebellar ataxia and in…
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1983
1983
Clinical features of monosomy 10qter.
A. Zatterale
,
L. Pagano
,
+5 authors
V. Ventruto
Annales de Genetique
1983
Corpus ID: 38860786
The authors report a 10qter deletion in a 16-month-old boy. The patient's phenotype includes: low birth weight, mental and growth…
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1983
1983
Expression of fragile site at 10q25 in normal culture conditions.
P. Petit
,
J. Fryns
American Journal of Human Genetics
1983
Corpus ID: 31272460
1981
1981
Heritable fragile sites on human chromosomes. VII. Children homozygous for the BrdU-requiring fra(10)(q25) are phenotypically normal.
Grant R. Sutherland
American Journal of Human Genetics
1981
Corpus ID: 28913060
A brother and sister have been detected who are homozygous for the bromodeoxyuridine (BrdU)-requiring fragile site at 10q25. The…
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1975
1975
Partial trisomy 10q occurring in a family with a reciprocal translocation t(10;18)(q25;q23).
S. Krøyer
,
E. Niebuhr
Annales de Genetique
1975
Corpus ID: 35232391
Partial trisomy 10q was observed in an eighteen year old girl with severe mental and physical retardation, microcephaly, a high…
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