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Chromosome 16 Short Arm

Known as: 16p, Chromosome 16 Proximal Arm 
Proximal (short) arm of chromosome 16
National Institutes of Health

Related topics

Related topics

14 relations
16p1116p11.216p11.2-12.116p11.2-p11.1

Papers overview

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Highly Cited
2006
Highly Cited
2006
High-Resolution Genomic Profiling Reveals Association of Chromosomal Aberrations on 1q and 16p with Histologic and Genetic Subgroups of Invasive Breast Cancer
Purpose: Invasive ductal carcinoma and invasive lobular carcinoma (ILC) represent the major histologic subtypes of invasive… 
Highly Cited
2006
Highly Cited
2006
Th1 Response and Cytotoxicity Genes Are Down-Regulated in Cutaneous T-Cell Lymphoma
Purpose: Increased production of Th2 cytokines characterizes Sezary syndrome, the leukemic form of cutaneous T-cell lymphomas… 
Highly Cited
2000
Highly Cited
2000
Identification of susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a two stage genome scan of affected sib-pairs
Abstract. Nonsyndromic cleft lip with or without cleft palate (CL/P) is a complex disorder of multigenic origin involving between… 
Highly Cited
2000
Highly Cited
2000
Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families
The role of genetic factors in the etiology of the autistic spectrum of disorders has clearly been demonstrated. Ten chromosomal… 
Highly Cited
1998
Highly Cited
1998
Results of a genome-wide genetic screen for panic disorder.
Panic disorder is characterized by spontaneous and recurrent panic attacks, often accompanied by agoraphobia. The results of… 
Highly Cited
1996
Highly Cited
1996
Duplication of a gene-rich cluster between 16p11.1 and Xq28: a novel pericentromeric-directed mechanism for paralogous genome evolution.
We have identified a 26.5 kb gene-rich duplication shared by human Xq28 and 16p11.1. Complete comparative sequence analysis of… 
Highly Cited
1996
Highly Cited
1996
Localisation of pseudohypoaldosteronism genes to chromosome 16p12.2-13.11 and 12p13.1-pter by homozygosity mapping.
Pseudohypoaldosteronism type 1 (PHA1, OMIM 264350) is a rare Mendelian disorder characterised by end-organ unresponsiveness to… 
Highly Cited
1995
Highly Cited
1995
Molecular characterization of 16p deletions associated with inversion 16 defines the critical fusion for leukemogenesis.
The inversion of chromosome 16 [inv(16)] in acute myeloid leukemia (AML) is associated with a p-arm deletion in a subset of… 
Highly Cited
1993
Highly Cited
1993
De novo truncation of chromosome 16p and healing with (TTAGGG)n in the alpha-thalassemia/mental retardation syndrome (ATR-16).
We have previously described a series of patients in whom the deletion of 1-2 megabases (Mb) of DNA from the tip of the short arm… 
Highly Cited
1992
Highly Cited
1992
Extensive cross-homology between the long and the short arm of chromosome 16 may explain leukemic inversions and translocations.
Specific rearrangements of chromosome 16 are well known in acute nonlymphocytic leukemia with abnormal eosinophils. While mapping… 
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