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1q32-q41

A chromosome band present on 1q
National Institutes of Health

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4 relations
CENPF wt AlleleChromosomesHSD11B1 wt Allelechromosome 1q

Papers overview

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2014
2014
[Identification of chromosomal aberration in esophageal cancer cells by mixed BAC DNA probes of chromosome arms and regions].
Chromosomal aberration is an important genetic feature of malignant tumor cells. This study aimed to clarify whether BAC DNA… 
2014
2014
Abstract 52: Identification of genomic alterations associated with metastasis in clear cell renal cell carcinoma
Clear cell renal cell carcinoma (ccRCC) is the most abundant and lethal form of RCC and about one third of patients exhibit… 
2010
2010
Polymorphism of Van der Woude Syndrome and Its Symptom Intensification in Subsequent Generations
Background. Van der Woude syndrome is characterized by such developmental malformations as lower lip sinuses/fistulas and cleft… 
2002
2002
Identifizierung differenziell exprimierter Gene bei Brust- und Ovarialkarzinomen in den chromosomalen Regionen 1q32-q41 und 11q12-q23
2000
2000
1q32-q41 microdeletion with reference to Van der Woude syndrome and allied clefting entities.
1999
1999
Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait.
van der Woude syndrome (vWS, MIM 119300) is a rare autosomal dominant clefting condition with cardinal features of mucous cysts… 
1996
1996
Refinement of the Van der Woude gene location and construction of a 3.5-Mb YAC contig and STS map spanning the critical region in 1q32-q41.
Van der Woude syndrome (VWS) is the most frequent form of syndromic clefting. Linkage analysis has localized the gene between… 
Review
1996
Review
1996
Survey of CAG/CTG repeats in human cDNAs representing new genes: candidates for inherited neurological disorders.
Expansion of polymorphic CAG and CTG repeats in transcripts is the cause of six inherited neurodegenerative or neuromuscular… 
1991
1991
The human tropomyosin gene involved in the generation of the TRK oncogene maps to chromosome 1q31.
The chromosomal localization of hTMnm, a gene coding for a cytoskeletal tropomyosin non-muscle isoform involved in the activation… 
1990
1990
Human TRK proto-oncogene maps to chromosome 1q32-q41.
The chromosomal localization of TRK, a gene coding for a putative receptor molecule with an associated tyrosine kinase activity… 
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