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5q35.2
A chromosome band present on 5q
National Institutes of Health
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5 relations
Chromosomes
HRH2 wt Allele
STC2 wt Allele
UIMC1 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
[Clinical phenotypes and a genetic analysis of patients with Sotos syndrome].
Min Zhao
Zhongguo dang dai er ke za zhi = Chinese journal…
2018
Corpus ID: 49679794
Three boys aged 7-13 months visited the hospital due to unusual facies (prominent forehead, hypertelorism, or long mandible…
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Review
2018
Review
2018
Cervical Spine Malformations Associated With a 5q34-5q35.2 Micro-interstitial Deletion: A Case Report
Hee-Dea Lee
,
J. Kim
,
S. Lim
,
B. Sul
,
B. Hong
Annals of Rehabilitation Medicine
2018
Corpus ID: 57783481
We report a female proband carrying a de novo 5q34-q35.2 deletion breakpoint, and review the unique skeletal phenotype and…
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2015
2015
Novel mutation detection of fibroblast growth factor receptor 1 (FGFR1) gene, FGFR2IIIa, FGFR2IIIb, FGFR2IIIc, FGFR3, FGFR4 gene for craniosynostosis: A prospective study in Asian Indian patient
Mayadhar Barik
,
M. Bajpai
,
A. Malhotra
,
J. Samantaray
,
S. Dwivedi
,
Sambhunath Das
Journal of Pediatric Neurosciences
2015
Corpus ID: 6052260
Background: Craniosynostosis (CS) syndrome is an autosomal dominant condition classically combining craniosynostosis and non…
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Review
2012
Review
2012
Author's response to reviews Title: Bilateral radial agenesis with absent thumbs, complex heart defect, short stature, and facial dysmorphism in a patient with pure distal microduplication of 5q35.2…
A. Jamsheer
,
A. Sowińska
,
T. Trzeciak
2012
Corpus ID: 117896262
2011
2011
Ventricular noncompaction and absent thumbs in a newborn with tetrasomy 5q35.2‐5q35.3: An association with Hunter–McAlpine syndrome?
E. Sellars
,
S. Zimmerman
,
T. Smolarek
,
R. Hopkin
American Journal of Medical Genetics. Part A
2011
Corpus ID: 19925858
We report on an infant with tetrasomy of 5q35.2‐5q35.3, an interstitial triplication on one chromosome and normal complement on…
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2001
2001
Girl with phenotypic abnormalities and a de novo, apparently balanced translocation 46,XX,t(5;10)(q35.2q11.2).
G. Zhu
,
G. Gillessen‐Kaesbach
,
J. Wirth
,
E. Passarge
,
O. Bartsch
American journal of medical genetics
2001
Corpus ID: 45189424
We describe a three-year-old girl with a triangular face, epicanthus, midfacial hypoplasia, apparently low-set ears, a small…
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2000
2000
Assignment of human xylosylprotein beta-1,4-galactosyltransferase gene (B4GALT7) to human chromosome 5q35.2-->q35.3 by in situ hybridization.
A. Kuroiwa
,
Y. Matsuda
,
T. Okajima
,
K. Furukawa
Cytogenetics and Cell Genetics
2000
Corpus ID: 33696165
1997
1997
Human inner ear OCP2 cDNA maps to 5q22-5q35.2 with related sequences on chromosomes 4p16.2-4p14, 5p13-5q22, 7pter-q22, 10 and 12p13-12qter.
Y. Liang
,
H. Chen
,
J. H. Asher
,
C. Chang
,
T. Friedman
Gene
1997
Corpus ID: 44642007
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