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Recent "Heterozygote" articles

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An initiation site for meiotic gene conversion in the yeast Saccharomyces cerevisiae
A Nicolas et al.
Nature 338 (6210), 35-9 (02 Mar 1989)
 
Dominant lethality of the mouse skeletal mutation tail-short (Ts) is determined by the Ts allele from mating partners
J Ishijima et al.
Genomics 49 (3), 341-50 (01 May 1998)
 
Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulation
Valerie L R M Verstraeten et al.
Human molecular genetics 15 (16), 2509-22 (15 Aug 2006)
 
Accelerated ageing in mice deficient in Zmpste24 protease is linked to p53 signalling activation
Ignacio Varela et al.
Nature, published online 22 Sep 2005
 
Targeted mutation of plasma phospholipid transfer protein gene markedly reduces high-density lipoprotein levels
X C Jiang et al.
The Journal of clinical investigation 103 (6), 907-14 (Mar 1999)
 
Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice
Loren G Fong et al.
Proceedings of the National Academy of Sciences of the United States of America 101 (52), 18111-6 (28 Dec 2004)
 
A homozygous ZMPSTE24 null mutation in combination with a heterozygous mutation in the LMNA gene causes Hutchinson-Gilford progeria syndrome (HGPS): insights into the pathophysiology of HGPS
Jonas Denecke et al.
Human mutation 27 (6), 524-31 (Jun 2006)
 
The exon 13 duplication in the BRCA1 gene is a founder mutation present in geographically diverse populations. The BRCA1 Exon 13 Duplication Screening Group
American journal of human genetics 67 (1), 207-12 (Jul 2000)
0002-9297 Journal Article Label: 10
 
Automating resequencing-based detection of insertion-deletion polymorphisms
Tushar Bhangale, Matthew Stephens, and Deborah Nickerson
Nature genetics, published online 19 Nov 2006
 
Reciprocal congenics defining individual quantitative trait Loci for sedative/hypnotic sensitivity to ethanol
B Bennett et al.
Alcoholism, clinical and experimental research 26 (2), 149-57 (Feb 2002)

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