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Chromosomes, Human, Pair 22

Known as: 22s chromosome, 22 chromosome, chromosome pair 22 
The designation for each member of the smallest human autosomal chromosome pair. Chromosome 22 spans about 49 million base pairs and represents… 
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
Out of Africa Kidney disease is more common in African Americans than in Americans of European descent, and genetics is likely to… 
Highly Cited
2002
Highly Cited
2002
The cytidine (C) to uridine (U) editing of apolipoprotein (apo) B mRNA is mediated by tissue-specific, RNA-binding cytidine… 
Review
2000
Review
2000
Chronic myeloid leukemia (CML) is probably the most extensively studied human malignancy. The discovery of the Philadelphia (Ph… 
Highly Cited
1999
Highly Cited
1999
Knowledge of the complete genomic DNA sequence of an organism allows a systematic approach to defining its genetic components… 
Highly Cited
1993
Highly Cited
1993
Neurofibromatosis type 2 (NF2) is a monogenic dominantly inherited disease predisposing carriers to develop nervous system… 
Highly Cited
1992
Highly Cited
1992
EWING'S sarcoma and related subtypes of primitive neuroectodermal tumours share a recurrent and specific t(ll;22) (q24;q12… 
Highly Cited
1985
Highly Cited
1985
Human chronic myelogenous leukaemia is characterized by a reciprocal translocation between chromosomes 9 and 22 resulting in an… 
Highly Cited
1985
Highly Cited
1985
The Philadelphia (Ph′) chromosome, an abnormal chromosome 22 (ref. 1), is one of the best-known examples of a specific human… 
Highly Cited
1973
Highly Cited
1973
CELLS from nine consecutive patients with chronic myelogenous leukaemia (CML) have been analysed with quinacrine fluorescence and…