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11p15

A chromosome band present on 11p
National Institutes of Health

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13 relations
ARNTL wt AlleleChromosome 11 Short ArmChromosomesFANCF wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2004
2004
Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases
SummaryTwo patients with trisomy 11p15 and features of Beckwith-Wiedemann syndrome are reported. The first is a female infant… 
2003
2003
Genetic and epigenetic alterations in sentinel lymph nodes metastatic lesions compared to their corresponding primary breast tumors.
2003
2003
Antenatal manifestation of congenital pancreatoblastoma in a fetus with Beckwith–Wiedemann syndrome
An Erratum has been published for this article in Prenatal Diagnosis 23(9) 2003, 771 
2001
2001
Genetic events during the transformation of a tamoxifen-sensitive human breast cancer cell line into a drug-resistant clone.
Review
2000
Review
2000
The molecular genetics of recurring chromosome abnormalities in acute myeloid leukemia.
  • Y. Hayashi
  • Seminars in hematology (Print)
  • 2000
  • Corpus ID: 7048011
1996
1996
Nonimmune fetal hydrops and placentomegaly: diagnosis of familial Wiedemann-Beckwith syndrome with trisomy 11p15 using FISH.
  • R. DrutR. Drut
  • American journal of medical genetics
  • 1996
  • Corpus ID: 30690833
We have studied a family in which four members of the same generation were affected with Wiedemann-Beckwith syndrome (WBS… 
1994
1994
Cytogenetic findings‐in 19 malignant bone tumors
Background. The majority of karyotypes observed in osteosarcomas (OS) and chondrosarcomas (CS) are complex, Specific chromosomal… 
1992
1992
Human casein kinase II subunit alpha: sequence of a processed (pseudo)gene and its localization on chromosome 11.
1991
1991
Allelic loss on the short arm of chromosome 11 in non‐small‐cell lung cancer
Forty‐eight samples of primary non‐small‐cell lung cancer (nsclc) and normal tissue from the same patients were analyzed for… 
1986
1986
Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma.
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