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2p13
A chromosome band present on 2p
National Institutes of Health
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Related topics
Related topics
6 relations
Chromosome 2 Short Arm
Chromosomes
DCTN1 wt Allele
DOK1 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
4q- Deletion Syndrome: Psychiatric Symptoms in a Rare Chromosomal Disorder
Maria Emília Pereira
,
Ricardo Caetano Silva
,
A. Velosa
,
B. Barahona-Corrêa
2016
Corpus ID: 77985021
We present the case of an 18-year-old man with the karyotype 46, XY, del (4) (q21.1q21.3), and describe in detail the clinical…
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2011
2011
Two cases with dysferlinopathy
G. Eryaşar
,
Y. Seçil
,
Y. Beckmann
,
Ayşen İnceoğlu Kendir
,
A. G. Diniz
,
M. Başoğlu
2011
Corpus ID: 196515575
Two Cases with Dysferlinopathy Gaye Eryaflar1, Yaprak Seçil1, Yeflim Beckmann1, Ayflen ‹nceo¤lu Kendir1, A. Gülden Diniz2…
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2009
2009
@bullet @bullet @bullet 43rd Annual Diagnostic Slide Session, 2002 References and Diagnoses
Moderator
,
Leroy R Tessa Hedley-Whyte
,
+7 authors
R. Greenwald
2009
Corpus ID: 11388095
Comment: This patient had been treated at one point in her course with intravenous immunoglobulin (IVIG), with no effect…
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2004
2004
Genome-Wide Linkage in a Large Dutch Consanguineous Family Maps a Locus for Intracranial Aneurysms to Chromosome 2 p 13
Y. Roos
,
G. Pals
,
+8 authors
A. Westerveld
2004
Corpus ID: 1365531
Background and Purpose—Familial occurrence of intracranial aneurysms suggests a genetic factor in the development of these…
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2003
2003
Amplifikace 2p13-16 u případu extranodálního velkobuněčnéhodifuzního B-lymfomu
K. Hušek
,
Petra Peťovská
,
D. Procházková
2003
Corpus ID: 185782481
2000
2000
Interspezies-Genom-Vergleich im Bereich des humanen Chr 2p13: Neue Kandidatengene für die neurologische Mutation wobbler der Maus
K. Resch
2000
Corpus ID: 162822648
1998
1998
Homology between human Chromosome 2p13.3 and the wobbler critical region on mouse Chromosome 11: comparative high-resolution mapping of STS and EST loci on YAC/BAC contigs
K. Resch
,
D. Korthaus
,
+6 authors
T. Schmitt-John
Mammalian Genome
1998
Corpus ID: 19287038
Abstract. Human Chr 2p13-14 and homologous regions on mouse Chrs 6 and 11 have been subjects of previous studies because they…
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1998
1998
Human DCTN1: genomic structure and evaluation as a candidate for Alström syndrome.
G. Collin
,
P. Nishina
,
J. Marshall
,
J. Naggert
Genomics
1998
Corpus ID: 10954009
The human dynactin 1 gene (DCTN1) is positioned on chromosome 2p13, the candidate region for various diseases including Alström…
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1992
1992
Multiple congenital anomalies due to partial 2p13----2pter duplication resulting from an unbalanced X;2 translocation.
P. Sarda
,
G. Lefort
,
P. Devaux
,
C. Humeau
,
D. Rieu
Annales de Genetique
1992
Corpus ID: 37155423
It has been suggested that partial distal 2p2----2pter duplication causes a relatively well defined clinical syndrome, mostly as…
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