Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 233,432,845 papers from all fields of science
Search
Sign In
Create Free Account
Chromosome 10 Short Arm
Known as:
10p
, Chromosome 10 Proximal Arm
Proximal (short) arm of chromosome 10
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
16 relations
10p11.1
10p11.2
10p11.21
10p11.23
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2001
Review
2001
Spitzoid malignant melanoma with lymph-node metastasis
D. Mihic-Probst
,
Jianming Zhao
,
P. Saremaslani
,
A. Baer
,
P. Komminoth
,
P. Heitz
Virchows Archiv
2001
Corpus ID: 23222248
Abstract. Distinction of spitzoid malignant melanomas (SMM) from Spitz nevi may be difficult or even impossible on the basis of…
Expand
2001
2001
Wrapping Up DiGeorge Syndrome in a T-box?
Min‐su Kim
,
C. Basson
Pediatric Research
2001
Corpus ID: 36231903
(DGS) is charac-terized by congenital heart diseasewith parathyroid and thymic hy-poplasia. Patients with related velocar…
Expand
1999
1999
Suggestive linkage of chromosome 10p to schizophrenia is not due to transmission ratio distortion.
S. Faraone
,
J. Meyer
,
+11 authors
M. Tsuang
American journal of medical genetics
1999
Corpus ID: 44335767
The genome scan of the European-American schizophrenia families from the Human Genetics Initiative of the National Institute of…
Expand
1998
1998
MRI findings in a patient with partial monosomy 10p.
Fay Sunada
,
F. C. Rash
,
David A Tam
,
David A Tam
Journal of Medical Genetics
1998
Corpus ID: 27919891
Partial monosomy 10p is a rare chromosomal disorder characterised by frontal bossing, micrognathia, congenital heart defects…
Expand
1986
1986
A patient with dup(10p)del(8q) and Pendred syndrome.
J. V. van Wouwe
,
M. Wijnands
,
P. Mourad‐Baars
,
J. Geraedts
,
G. Beverstock
,
J J van de Kamp
American journal of medical genetics
1986
Corpus ID: 45397014
We report on a severely retarded girl with multiple congenital anomalies. Chromosome studies showed a der (8) chromosome with dup…
Expand
1985
1985
Partial monosomy 10p syndrome.
R. Koenig
,
E. Kessel
,
W. Schoenberger
Annales de Genetique
1985
Corpus ID: 39189559
A newborn infant with monosomy 10p13 is reported. The clinical signs and symptoms of the present case are compared with those of…
Expand
1983
1983
Duplication 10p in a girl due to a maternal translocation t(10;14) (p11:p12).
C. H. González
,
A. Billerbeck
,
L. C. Takayama
,
A. Wajntal
American journal of medical genetics
1983
Corpus ID: 2364983
We present a dup (10p) due to a t(10;14) (p11;p12)mat with a malformation syndrome in a girl. The analysis of 37 published cases…
Expand
1981
1981
Trisomy 10p produced by recombination involving maternal inversion inv(10)(pllq26).
S. LANSKY-SHAFER
,
W. Daniel
,
L. Ruiz
Journal of Medical Genetics
1981
Corpus ID: 29252261
An infant with features of trisomy 10p syndrome was found to have an abnormal chromosome 10: 46, XY, rec(10), dup p, inv(10…
Expand
1978
1978
Partial trisomy 10p in two generations
I. Lurie
,
G. Lazjuk
,
D. B. Gurevich
,
G. I. Kravtzova
,
M. Nedzved
,
I. Shved
Human Genetics
1978
Corpus ID: 26707802
SummaryTwo cases of partial 10p trisomy due to a t(10;20)(p12;p12) in two generations of a family are presented. Analysis of 20…
Expand
1976
1976
[2 cases of partial trisomy 10p due to a paternal translocation t(10p;18)(p13;q23)].
S. Morić-Petrović
,
Ž. Laća
,
A. Krajgher
,
J. Milośevic
Annales de Genetique
1976
Corpus ID: 35632550
Two brothers trisomic for the distal two thirds of 10p are reported. Trisomy results from the malsegregation of a familial…
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