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9q34.3
A chromosome band present on 9q
National Institutes of Health
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Related topics
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11 relations
Chromosomes
EHMT1 wt Allele
MAPKAP1 wt Allele
NACC2 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2007
2007
Prenatal diagnosis of a 9q34.3 microdeletion by array‐CGH in a fetus with an apparently balanced translocation
Marcia J. Simovich
,
S. Yatsenko
,
+6 authors
J. Lupski
Prenatal Diagnosis
2007
Corpus ID: 21804755
Use high‐resolution genome analysis to clarify the genomic integrity in a fetus with a cytogenetically balanced translocation t(2…
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2006
2006
Genome‐wide linkage analysis of allergic rhinoconjunctivitis in a Swedish population
L. Bu
,
M. Bradley
,
C. Söderhäll
,
C. Wahlgren
,
I. Kockum
,
M. Nordenskjöld
Clinical and Experimental Allergy
2006
Corpus ID: 22668671
Background Allergic rhinoconjunctivitis is a common complex disorder characterized by itching and irritation in the nose, bouts…
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2004
2004
Functional analysis of the NPDC-1 gene.
C. Evrard
,
S. Caron
,
P. Rouget
Gene
2004
Corpus ID: 2978894
2002
2002
MIZIP, a highly conserved, vertebrate specific melanin‐concentrating hormone receptor 1 interacting zinc‐finger protein 1
D. Bächner
,
H. Kreienkamp
,
D. Richter
FEBS Letters
2002
Corpus ID: 9432075
2002
2002
Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations
M. Medlej‐Hashim
,
M. Mustapha
,
+8 authors
A. Mégarbané
European Journal of Human Genetics
2002
Corpus ID: 488988
Non-syndromic recessive deafness (NSRD) is the most commonly encountered form of hereditary hearing loss. The majority of NSRD…
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Highly Cited
1998
Highly Cited
1998
Exon scanning of the entire TSC2 gene for germline mutations in 40 unrelated patients with tuberous sclerosis
R. Beauchamp
,
Ashleigh Banwell
,
+7 authors
V. Ramesh
Human Mutation
1998
Corpus ID: 46522156
Tuberous sclerosis complex (TSC) is a dominantly inherited multisystem disorder resulting in the development of hamartomatous…
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Highly Cited
1997
Highly Cited
1997
Human Lysophosphatidic Acid Acyltransferase
C. Eberhardt
,
P. Gray
,
L. Tjoelker
Journal of Biological Chemistry
1997
Corpus ID: 31465493
Lysophosphatidic acid (1-acyl-sn-glycero-3-phosphate (LPA)) is a phospholipid with diverse biological activities. The mediator…
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1997
1997
Advances in molecular genetics of a-2- and a-3/4-fucosyltransferases
M. Costache
,
A. Cailleau
,
P. Fernández-Mateos
,
R. Oriol
,
R. Mollicone
1997
Corpus ID: 57623033
1992
1992
Mapping of the human COL5A1 gene to chromosome 9q34.3
G. Caridi
,
A. Pezzolo
,
+4 authors
G. Ghiggeri
Human Genetics
1992
Corpus ID: 12728165
SummaryA 353-bp region encoding for the NH2 terminus of the noncollagenic part of the αl(V) chain was amplified by the polymerase…
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1986
1986
High resolution banding analysis of the reciprocal translocation t(6;9) in acute nonlymphocytic leukemia.
S. Heim
,
U. Kristoffersson
,
+4 authors
T. Wiebe
Cancer Genetics and Cytogenetics
1986
Corpus ID: 3437135
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