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4q35.1

A chromosome band present on 4q
National Institutes of Health

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3 relations
ChromosomesING2 wt AlleleSORBS2 wt Allele

Papers overview

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2015
2015
Copy number variants associated with epilepsy from gene expression microarrays
2015
2015
Clinical and Molecular Delineation of a Novel De Novo 4q28.3-31.21 Interstitial Deletion in a Patient with Developmental Delay
The 4q deletion syndrome is a rare disorder, with an estimated incidence of 1 in 1000001 and approximately 150 patients have been… 
2014
2014
Loss of 4q21.23-22.1 Is a Prognostic Marker for Disease Free and Overall Survival in Non-Small Cell Lung Cancer
This study was performed to assess the prognostic relevance of genomic aberrations at chromosome 4q in NSCLC patients. We have… 
2013
2013
[Anaplastic large cell lymphoma: an array-based comparative genomic hybridization study].
OBJECTIVE To use array-based comparative genomic hybridization (aCGH) technology to study the molecular cytogenetic abnormalities… 
2012
2012
Molecular cytogenetic characterization of the first reported case of an inv dup (4p)(p15.1-pter) with a concomitant 4q35.1-qter deletion and normal parents.
2010
2010
Identification and molecular characterization of two novel chromosomal deletions associated with autism
Autism is a childhood-onset neurodevelopmental disorder with a strong genetic basis in its etiology. Conventional karyotype… 
2009
2009
Obesity syndrome, MOMES caused by deletion–duplication (4q35.1 del and 5p14.3 dup)
Obesity Syndrome, MOMES Caused by Deletion–Duplication (4q35.1 del and 5p14.3 dup) Mieke M. van Haelst, Rubin Wang, Piranit N… 
Review
2006
Review
2006
An unusual clinical characterization of a male with distal partial trisomy 1q42.1 and monosomy 4q35.1 and review of the literature.
We report a male patient with a karyotype of 46,XY, der(4)t(1;4)(q42.1;q35.1) inherited from a maternal balanced translocation… 
2004
2004
Generation of locus-specific probes for interphase fluorescence in situ hybridisation--application in Barrett's esophagus.
2004
2004
Deletions on chromosome 4 in sporadic and BRCA mutated tumors and association with pathological variables.
BACKGROUND Chromosomal aberrations in breast tumors from BRCA1 and BRCA2 germ-line mutation carriers are considerably more… 
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