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7q21.3-q22.1

A chromosome band present on 7q
National Institutes of Health

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4 relations
Chromosome 7qChromosomesMCM7 wt AlleleSHFM1 wt Allele

Papers overview

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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… 
2011
2011
Abstract 3908: Genomic profiling of gastric carcinoma in situ and adenomas by array-based comparative genomic hybridization
Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL Although genomic copy number aberrations (CNAs) of… 
2010
2010
Genomic profiling of gastric carcinoma in situ and adenomas by array‐based comparative genomic hybridization
Although genomic copy number aberrations (CNAs) of gastric carcinoma at the advanced stage have already been extensively… 
2006
2006
Paraoxonase-1 Q 192 R polymorphism and risk of sporadic amyotrophic lateral sclerosis
To the Editor: Paraoxonase-1 (PON1) is an HDL-associated enzyme which hydrolyzes the oxidized lipids in LDL and organophosphate… 
1999
1999
Cloning and characterization of two cytoplasmic dynein intermediate chain genes in mouse and human.
Cytoplasmic dynein is a large multisubunit microtubule-based motor protein, which mediates movement of numerous intracellular… 
1997
1997
New polymorphism and linkage mapping of the bovine lactotransferrin gene
Species: Mouse Locus name: deleted in split hand/split foot 1 Locus symbol: dssl Map position: 6A Method of mapping: Fluorescence… 
1997
1997
Fluorescent in situ mapping of the murine deleted in split hand/split foot 1 (dss1) gene to Chromosome 6
Species: Mouse Locus name: deleted in split hand/split foot 1 Locus symbol: dssl Map position: 6A Method of mapping: Fluorescence… 
1996
1996
Genetics of split hand and split foot. A case study.
  • B. D. Caldwell
  • Journal of the American Podiatric Medical…
  • 1996
  • Corpus ID: 22323750
Split hand and split foot is an autosomal dominant disorder that displays several genetic phenomena. These include variable… 
1994
1994
Familial split hand/split foot long bone deficiency does not segregate with markers linked to the SHFD1 locus in 7q21.3-q22.1.
Ectrodactyly (split hand/split foot, SHSF) is characterized by the absence of middle rays of the hand or the foot. Cytogenetic… 
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