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Chromosomes, Human, Pair 11

Known as: Chromosome 11 
The designation for each member of the eleventh largest human autosomal chromosome pair. Chromosome 11 spans about 134.5 million base pairs and… 
National Institutes of Health

Related topics

Related topics

50 relations
Adult Kidney Wilms TumorAleukemic Chronic Lymphocytic LeukemiaAnaplastic Kidney Wilms TumorBeckwith-Wiedemann Syndrome

Narrower (2)

Chromosome 11p deletion syndromechromosome 11q duplication syndrome

Broader (2)

Chromosomes, HumanChromosomes, Human, 6-12 and X

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2004
Highly Cited
2004
Late Breaking Science Abstracts
The Late Breaking Science abstracts were originally presented at the 57th American Academy of Neurology Annual Meeting in San… 
Review
1996
Review
1996
Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.
The congenital long-QT syndrome (LQTS) is characterized by prolonged QT intervals, QT interval lability, and polymorphic… 
Highly Cited
1996
Highly Cited
1996
Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemia
Expression of HoxaT and Hoxa9 is activated by proviral integration in BXH2 murine myeloid leukaemias. This result, combined with… 
Highly Cited
1994
Highly Cited
1994
New member of the winged-helix protein family disrupted in mouse and rat nude mutations
Highly Cited
1993
Highly Cited
1993
Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour
GENOMIC imprinting has been implicated in the onset of several embryonal tumours but the mechanism is not well understood1–3… 
Highly Cited
1992
Highly Cited
1992
The gene for the peripheral myelin protein PMP–22 is a candidate for Charcot–Marie–Tooth disease type 1A
Charcot–Marie-–ooth disease type 1A (CMT1A) is an autosomal dominant peripheral neuropathy associated with a large DNA… 
Highly Cited
1991
Highly Cited
1991
Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene.
Genetic factors contribute to heart disease. In this study, linkage analyses have been performed in a family that is predisposed… 
Highly Cited
1990
Highly Cited
1990
High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones.
Cosmid clones containing human DNA inserts have been mapped on chromosome 11 by fluorescence in situ hybridization under… 
Highly Cited
1989
Highly Cited
1989
LINKAGE BETWEEN IMMUNOGLOBULIN E RESPONSES UNDERLYING ASTHMA AND RHINITIS AND CHROMOSOME 11q
Highly Cited
1978
Highly Cited
1978
Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion.
The triad of aniridia, ambiguous genitalia, and mental retardation (AGR triad) is the characteristic clinical feature of three… 
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