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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

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Highly Cited
1996
Highly Cited
1996
Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach
The Changes in the type of haemoglobin (Hb) produced during embryonic, fetal and adult life, have served as a paradigm for… 
Highly Cited
1996
Highly Cited
1996
Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11.
A contiguous gene syndrome due to deletions of the proximal short arm of chromosome 11 is described in eight patients belonging… 
Highly Cited
1989
Highly Cited
1989
A fine-structure deletion map of human chromosome 11p: Analysis of J1 series hybrids
Deletion analysis offers a powerful alternative to linkage and karyotypic approaches for human chromosome mapping. A panel of… 
Highly Cited
1989
Highly Cited
1989
Evidence for genetic heterogeneity in tuberous sclerosis.
The question of genetic heterogeneity in tuberous sclerosis (TSC) was addressed by genetic linkage studies in eight affected… 
Highly Cited
1985
Highly Cited
1985
Expression of homologous homeo-box-containing genes in differentiated human teratocarcinoma cells and mouse embryos
Highly Cited
1985
Highly Cited
1985
Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome.
We describe five individuals who have constitutional deletions of the short arm of one chromosome 11, including all or part of… 
Highly Cited
1985
Highly Cited
1985
Chromosome 11 aberrations in small colony L5178Y TK-/- mutants early in their clonal history.
Highly Cited
1985
Highly Cited
1985
The human Thy-1 gene: structure and chromosomal location.
The human Thy-1 gene has been isolated and sequenced and compared to the rat and mouse Thy-1 genes. All three genes are organized… 
Highly Cited
1984
Highly Cited
1984
Nonrandom chromosomal changes in transitional cell carcinoma of the bladder.
Nine cases of transitional cell carcinoma (eight from the urinary bladder and one from the ureter; six noninvasive and three… 
Highly Cited
1983
Highly Cited
1983
Oncogene from human EJ bladder carcinoma is located on the short arm of chromosome 11.
The human cellular homolog of the transforming DNA sequence isolated from the bladder carcinoma cell line EJ was localized on the… 
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