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Maxillary left third molar prosthesis

Known as: 16p 
National Institutes of Health

Papers overview

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2017
2017
Preparation, Microstructure Evolutions, and Mechanical Property of an Ultra-Fine Grained Mg-10Gd-4Y-1.5Zn-0.5Zr Alloy
In this work, the microstructural evolutions and mechanical properties of an as-cast Mg-10Gd-4Y-1.5Zn-0.5Zr (wt %) alloy during… 
2007
2007
Refinement of the genetic cause of ATR-16
Alpha thalassemia retardation associated with chromosome16 (ATR-16 syndrome) is defined as a contiguous gene syndrome resulting… 
2006
2006
Linkage analysis of rheumatoid arthritis in US and UK families reveals interactions between HLA-DRB1 and loci on chromosomes 6q and 16p.
OBJECTIVE HLA is the most strongly associated locus in rheumatoid arthritis (RA), accounting for up to one-third of the genetic… 
2005
2005
Copy number gains on 22q13 in adenoid cystic carcinoma of the salivary gland revealed by comparative genomic hybridization and tissue microarray analysis.
Review
2002
Review
2002
Comparative genomic hybridisation shows a partial de novo deletion 16p11.2 in a neonate with multiple congenital malformations
Chromosome alterations, including numerical and structural chromosome rearrangements, are implicated in abnormal fetal… 
1995
1995
Chromosome microdissection identifies cryptic sites of DNA sequence amplification in human ovarian carcinoma.
DNA sequence amplification contributes to the multistep process of carcinogenesis, and overexpression of amplified genes has been… 
1994
1994
Linkage disequilibrium between the juvenile neuronal ceroid lipofuscinosis gene and marker loci on chromosome 16p12.1
The neuronal ceroid lipofuscinoses (NCL; Batten disease) are a collection of autosomal recessive disorders characterized by the… 
Review
1992
Review
1992
Trisomy 16p in a liveborn infant and review of trisomy 16p.
We report on an infant boy with duplication of part of 16p and partial deficiency of 9p: 46,XY, -9, + der(9)t(9;16)(p24;p13.1)mat… 
1992
1992
An unusually large (CA)n repeat in the region of divergence between subtelomeric alleles of human chromosome 16p.
1985
1985
Chondrodysplasia punctata in an infant with duplication 16p due to a 7;16 translocation.
This paper describes a newborn with a number of clinical manifestations compatible with duplication 16p due to a 46, XY, -7, +der… 
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