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1q42

A chromosome band present on 1q
National Institutes of Health

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5 relations
ChromosomesPARP1 wt AlleleTOMM20 wt AlleleWNT9A wt Allele

Papers overview

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Review
2015
Review
2015
ReviewEpilepsy and chromosomal abnormalities
Background: Many chromosomal abnormalities are associated with Central Nervous System (CNS) malformations and other neurological… 
2007
2007
Genetic Determination of Osteoporosis: Lessons Learned from a Large Genome-Wide Linkage Study
ABSTRACT Osteoporosis is a common disease with strong genetic control. We performed an autosomal linkage scan in a large pedigree… 
Review
1989
Review
1989
A new case of deletion 1q42 syndrome
We report a 1 8/12‐year‐old male with a de novo deletion of 1q42. The case is compared with 23 others from the literature. The… 
1986
1986
Chromosome deletion 1q42-43.
We report on a newborn male and a female of 3 years 9 months with de novo 1q42 or 43-qter deletions. These cases are compared… 
1986
1986
DAPI-inducible common fragile sites.
DAPI, a compound specific for the AT bases of DNA, causes gaps and breaks in three human chromosome sites, at the 1q41-1q42… 
1983
1983
[Distal 1q monosomy. 2 new cases and description of the syndrome].
In two unrelated girls, each with severe mental deficiency and craniofacial dysmorphism, deletion of chromosome segment 1q4 had… 
1982
1982
A 1q42 deletion in a Vietnamese infant.
1982
1982
A 1q42 deletion in a Vietnamese infant.
1982
1982
Regional assignment of the structural gene for human acid beta-glucosidase to q42 leads to qter on chromosome 1.
The structural gene for human acid beta-glucosidase (GBA) has been regionally assigned to a narrow region on chromosome 1 using… 
1981
1981
New deletion syndrome: 1q43.
A male infant showed dysmorphology of the head and face, neck, extremities, and genitalia, as well as growth and mental…