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9p22.3
A chromosome band present on 9p
National Institutes of Health
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Related topics
Related topics
3 relations
Chromosome 9 Short Arm
Chromosomes
SMARCA2 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Evidence that homozygous PTPRD gene microdeletion causes trigonocephaly, hearing loss, and intellectual disability
Nancy Choucair
,
Cécile Mignon‐Ravix
,
+5 authors
E. Chouery
Molecular Cytogenetics
2015
Corpus ID: 10631618
BackgroundThe premature fusion of metopic sutures results in the clinical phenotype of trigonocephaly. An association of this…
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2013
2013
Gene copy number variations in breast cancer of Sub-Saharan African women.
M. Ly
,
A. Valent
,
+11 authors
F. André
Breast
2013
Corpus ID: 206350703
2013
2013
7q36 deletion and 9p22 duplication: effects of a double imbalance
Karla de Oliveira Pelegrino
,
S. Sugayama
,
Ana Lúcia Catelani
,
Karina Lezirovitz
,
F. Kok
,
M. Chauffaille
Molecular Cytogenetics
2013
Corpus ID: 5132343
The etiology of mental retardation/developmental delay (MRDD) remains a challenge to geneticists and clinicians and can be…
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2012
2012
Partial monosomy 9p (9p22.2-->pter) and partial trisomy 18q (18q21.32-->qter) in a female infant with anorectal malformations.
C. Chen
,
H.‐M. Lin
,
+5 authors
W. Wang
Genetic Counseling
2012
Corpus ID: 37824278
We report a female infant with a karyotype of 46,XX,der(9)t(9;18)(p22.2;q21.32)pat and the phenotypic features of craniofacial…
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Highly Cited
2011
Highly Cited
2011
Heterozygous Mutations of FREM1 Are Associated with an Increased Risk of Isolated Metopic Craniosynostosis in Humans and Mice
L. Vissers
,
T. C. Cox
,
+19 authors
T. Roscioli
PLoS Genetics
2011
Corpus ID: 2388776
The premature fusion of the paired frontal bones results in metopic craniosynostosis (MC) and gives rise to the clinical…
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2010
2010
A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation
K. Abu-Amero
,
A. Hellani
,
+4 authors
T. Bosley
BMC Medical Genetics
2010
Corpus ID: 8053713
BackgroundPrevious studies focusing on candidate genes and chromosomal regions identified several copy number variations (CNVs…
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2009
2009
Potential predictive markers of chemotherapy resistance in stage III ovarian serous carcinomas
L. Österberg
,
K. Levan
,
+4 authors
G. Horvath
BMC Cancer
2009
Corpus ID: 16890185
BackgroundChemotherapy resistance remains a major obstacle in the treatment of women with ovarian cancer. Establishing predictive…
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2008
2008
NFIB rearrangement in superficial, retroperitoneal, and colonic lipomas with aberrations involving chromosome band 9p22
A. Italiano
,
N. Ebran
,
+5 authors
F. Pedeutour
Genes, Chromosomes and Cancer
2008
Corpus ID: 20985812
Lipomas are frequently characterized by rearrangements resulting in the fusion of the HMGA2 gene (12q14.3) with a variety of…
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2005
2005
Is loss of heterozygosity at 9q22.3 (PTCH gene) and 19p13.3 (STK11 gene) involved in the pathogenesis of ovarian stromal tumors?
T. Tsuji
,
L. Catasús
,
J. Prat
Human Pathology
2005
Corpus ID: 2998246
Highly Cited
2003
Highly Cited
2003
Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.
R. Segurado
,
S. Detera-Wadleigh
,
+75 authors
N. Akarsu
American Journal of Human Genetics
2003
Corpus ID: 10008887
Genome scans of bipolar disorder (BPD) have not produced consistent evidence for linkage. The rank-based genome scan meta…
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