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del(1p36)

Known as: 1p36 Deletion, Loss of Chromosome 1p36 
A chromosomal deletion involving the p36 band of chromosome 1. This deletion is associated with 1p36 deletion syndrome.
National Institutes of Health

Related topics

Related topics

14 relations
Chromosomes, Human, Pair 1Localized ChondrosarcomaMerkel cell carcinomaMetastatic Chondrosarcoma

Papers overview

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Highly Cited
2015
Highly Cited
2015
Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes.
Highly Cited
2013
Highly Cited
2013
Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.
Highly Cited
2010
Highly Cited
2010
Mig-6 controls EGFR trafficking and suppresses gliomagenesis
Glioblastoma multiforme (GBM) is the most common and lethal primary brain cancer that is driven by aberrant signaling of growth… 
Highly Cited
2008
Highly Cited
2008
Spectrum of epilepsy in terminal 1p36 deletion syndrome
Purpose: Previous reports have summarized the seizures types occurring in 1p36 deletion syndrome. To better define the spectrum… 
Review
2007
Review
2007
Monosomy 1p36 deletion syndrome
Monosomy 1p36 results from a heterozygous deletion of the most distal chromosomal band on the short arm of chromosome 1… 
Highly Cited
2007
Highly Cited
2007
Genetic and epigenetic changes in the common 1p36 deletion in neuroblastoma tumours
Chromosome 1p is frequently deleted in neuroblastoma (NB) tumours. The commonly deleted region has been narrowed down by loss of… 
Highly Cited
2001
Highly Cited
2001
Loss of the Potassium Channel β‐Subunit Gene, KCNAB2, Is Associated with Epilepsy in Patients with 1p36 Deletion Syndrome
Summary:  Purpose: Clinical features associated with chromosome 1p36 deletion include characteristic craniofacial abnormalities… 
Highly Cited
1999
Highly Cited
1999
Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletions.
The deletion of chromosome 1p36 is a newly recognized, relatively common contiguous gene deletion syndrome with a variable… 
Highly Cited
1996
Highly Cited
1996
Additional copies of a 25 Mb chromosomal region originating from 17q23.1‐17qter are present in 90% of high‐grade neuroblastomas
Neuroblastoma shows remarkable heterogeneity, ranging from spontaneous regression to progression toward highly malignant tumors… 
Highly Cited
1993
Highly Cited
1993
Constitutional 1p36 deletion in a child with neuroblastoma.
We describe a child with dysmorphic features, as well as developmental and growth delay, who developed neuroblastoma at 5 mo of… 
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