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21q21.3

A chromosome band present on 21q
National Institutes of Health

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21qAPP wt AlleleChromosomes

Papers overview

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2020
2020
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification
2015
2015
Replication the association of 2q32.2-q32.3 and 14q32.11 with hepatocellular carcinoma.
Highly Cited
2010
Highly Cited
2010
Detailed molecular and clinical characterization of three patients with 21q deletions
Lindstrand A, Malmgren H, Sahlén S, Schoumans J, Nordgren A, Ergander U, Holm E, Anderlid BM,Blennow E. Detailed molecular and… 
2003
2003
The donor chromosome breakpoint for a jumping translocation is associated with large low-copy repeats in 21q21.3
Jumping translocations (JTs) are very rare chromosome aberrations, usually identified in tumors. We report a constitutional JT… 
Highly Cited
1998
Highly Cited
1998
A novel C-terminal binding protein (CTBP2) is closely related to CTBP1, an adenovirus E1A-binding protein, and maps to human chromosome 21q21.3.
A region of the C-terminus of adenovirus type 2/5 E1A protein has been associated with negative modulation of tumorigenicity, as… 
1995
1995
Physical findings in 21q22 deletion suggest critical region for 21q- phenotype in q22.
Multiple abnormalities were observed in a newborn infant with a deletion in the long arm of chromosome 21, from band 22q22.1… 
Highly Cited
1992
Highly Cited
1992
Mapping of a gene predisposing to early–onset Alzheimer's disease to chromosome 14q24.3
Genetic linkage studies with chromosome 21 DNA markers and mutation analysis of the β–amyloid protein precursor gene located in… 
1992
1992
Isolation, characterization, and regional mapping of microclones from a human chromosome 21 microdissection library.
Thirty-four unique-sequence microclones were isolated from a previously described microdissection library of human chromosome 21… 
1990
1990
A familial interstitial deletion of the long arm of chromosome 21
A mother and daughter with an interstitial deletion of the chromosome segment 21q11 to 21q2l.3 have similar minor dysmorphism and… 
1977
1977
Partial trisomy 20 (20q13) and partial trisomy 21 (21pter leads to 21q21.3).
A patient with a double partial trisomy 20 and 21 with mild mental retardation and multiple congenital anomalies is presented… 
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