Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 225,058,997 papers from all fields of science
Search
Sign In
Create Free Account
Xq26-q28
A chromosome band present on Xq
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
2 relations
BRS3 wt Allele
Chromosomes
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
1995
1995
Severe haemophilia A in a female resulting from two de novo factor VIII mutations
S. Windsor
,
Ann Lyng
,
S. Taylor
,
B. Ewenstein
,
E. Neufeld
,
D. Lillicrap
British Journal of Haematology
1995
Corpus ID: 20562368
Summary. A 2‐year‐old girl is described with severe haemophilia A (factor VIII: C <0‐01 units/ml). Both of her parents were…
Expand
Review
1993
Review
1993
[Laser chromosome microdissection and cloning of the genetic disease loci].
S. Hadano
,
J. Ikeda
Nihon rinsho. Japanese journal of clinical…
1993
Corpus ID: 38861918
We have developed an argon ion laser chromosome microdissection technique in conjunction with a single unique primer polymerase…
Expand
1992
1992
Tentative assignment of gene for oto-palato-digital syndrome to distal Xq (Xq26-q28).
D. Hoar
,
L. Field
,
F. Beards
,
G. Hoganson
,
B. Rollnick
,
J. Hoo
American journal of medical genetics
1992
Corpus ID: 21262420
Detailed physical mapping of oto-palato-digital (OPD) syndrome gene on the X-chromosome was attempted on a family of 3…
Expand
1991
1991
Linkage homogeneity near the fragile X locus in normal and fragile X families.
G. Suthers
,
J. Mulley
,
+7 authors
S. Thibodeau
Genomics
1991
Corpus ID: 12325090
1989
1989
Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304).
N. Dahl
,
P. Goonewardena
,
+6 authors
U. Pettersson
American Journal of Human Genetics
1989
Corpus ID: 28265139
A new polymorphic DNA marker U6.2, defining the locus DXS304, was recently isolated and mapped to the Xq27 region of the X…
Expand
1988
1988
Biologie moleculaire de maladies liees au chromosome x : localisation des genes responsables de trois immunodeficiences et de deux formes de retard mental non specifique, cartographie genetique et…
B. Arveiler
1988
Corpus ID: 82622456
1987
1987
Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26–q27
I. Oberle
,
G. Camerino
,
+4 authors
J. Mandel
Human Genetics
1987
Corpus ID: 2190907
SummaryThe q26–q28 region of the human X chromosome contains several important disease loci, including the locus for the fragile…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE