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9q34.1

A chromosome band present on 9q
National Institutes of Health

Papers overview

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Review
2009
Review
2009
Citrullinemia type I is an autosomal recessive disorder that is caused by a deficiency of the urea cycle enzyme argininosuccinate… 
2005
2005
Correction to: Laboratory Investigation (2005) 85, 895–907. doi:10.1038/sj.labinvest.3700268 Following the publication of the… 
Highly Cited
2000
Highly Cited
2000
Nail-patella syndrome is an autosomal dominant disorder characterized by dyplasia of finger nails, skeletal anomalies, and… 
Highly Cited
1999
Highly Cited
1999
We have isolated a human gene homologous to Drosophila melanogaster rotated abdomen, rt, a poorly viable recessive mutation… 
Highly Cited
1997
Highly Cited
1997
Idiopathic torsion dystonia is characterized by involuntary twisting movements and postures. One molecularly defined form with… 
Highly Cited
1995
Highly Cited
1995
DAP-kinase (DAPK) and DAP1 were recently identified as positive mediators of IFN-{gamma}-induced programmed cell death. The… 
Highly Cited
1990
Highly Cited
1990
XERODERMA pigmentosum (XP) is an autosomal recessive disease, characterized by a high incidence of sunlight-induced skin cancer…