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10p13

A chromosome band present on 10p
National Institutes of Health

Related topics

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4 relations
CELF2 wt AlleleChromosome 10 Short ArmChromosomesDCLRE1C wt Allele

Papers overview

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2018
2018
Terminal deletion of chromosome 10p13 as a cause of hypoparathyroidism in a neonate
Objective – To present a case of hypoparathyroidism that was found to be a part of a rare chromosomal syndrome and to emphasize… 
2005
2005
A Quantitative Trait Locus For Maximal Exercise Heart Rate On Chromosome 10p13: The Heritage Family Study
2001
2001
KUOPION YLIOPISTO UNIVERSITY OF KUOPIO
Alzheimer’s disease (AD) is the most common cause of progressive neurological disorder leading to dementia. It is… 
1996
1996
Progressive deficiencies in blood T cells associated with a 10p12-13 interstitial deletion.
We report on a 8-year-old patient affected by a selective T-cell defect associated with mental retardation and dysmorphic signs… 
1994
1994
Comparison of facial features of DiGeorge syndrome (DGS) due to deletion 10p13-10pter with DGS due to 22q11 deletion
DiGeorge syndrome (DGS) is a congenital anomaly consisting of cardiac defects, aplasia or hypoplasia of the thymus and parathroid… 
1986
1986
Congenital monoblastic leukemia cutis. A case report with chromosomal abnormality: del (10p).
Congenital monoblastic leukemia cutis is a rare disorder. We report an infant who developed infiltrative skin lesions by 2 weeks… 
1985
1985
Partial monosomy 10p syndrome.
A newborn infant with monosomy 10p13 is reported. The clinical signs and symptoms of the present case are compared with those of… 
Review
1983
Review
1983
Partial monosomy of chromosome 10 short arms.
Two children with monosomy 10p13 are reported. In the first case the monosomy was the result of a maternal balanced translocation…