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© 1997 Nature Publishing Group http://www.nature.com/naturegenetics
MLH1 and MSH2 - Hindawi Publishing Corporation · 2019. 7. 30. · Research Article Novel Mutations in MLH1 and MSH2 Genes in Mexican Patients with Lynch Syndrome JoseMiguelMoreno-Ortiz,
Novel Splicing, Missense, and Deletion Mutations in Seven ...dm5migu4zj3pb.cloudfront.net/manuscripts/116000/116833/JCI9311… · Novel Splicing, Missense, and Deletion Mutations
Comprehensive Analysis of Missense Variations - Cancer Research
A missense mutation in ITGB6 causes pitted …eprints.whiterose.ac.uk/80650/1/A missense mutation in ITGB6 causes... · ameloblast-ameloblast interactions and proteolytic processing
Empirical Evidence for Heterozygote Advantage in …...2016/05/16 · Empirical evidence for heterozygote advantage in adapting diploid populations of Saccharomyces cerevisiae Diamantis
BAP1 Missense Mutation c.2054 A>T (p.E685V) Completely
Class III Malocclusion: Missense Mutations in DUSP6 Gene
Lipoprotein profiles in human heterozygote carriers of a …liu.diva-portal.org/smash/get/diva2:872193/FULLTEXT01.pdf · 2016-03-11 · Lipoprotein profiles in human heterozygote
Massively parallel functional analysis of missense
Missense mutation in the ATPase ... - yoksis.bilkent.edu.tr
A Heterozygous Missense Variant in MAP2K2 in a Stillborn
BRCA2 Hypomorphic Missense Variants Confer Moderate … CLUB DEVILEE... · BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer Hermela Shimelis1, Romy L.S
Missense Mutations in the Homeodomain of HOXD13 Are Associated
Functional characterization of DYRK1A missense variants ... · Functional characterization of DYRK1A missense variants associated with a syndromic form of intellectual deficiency
Predicting the impact of Lynch syndrome-causing missense ......RESEARCH ARTICLE Predicting the impact of Lynch syndrome-causing missense mutations from structural calculations Sofie
Missense mutations in the SH3TC2 protein causing Charcot-Marie
Identification of missense mutation (G365R) of the butyrylcho
Patterns of recombination and MLH1 foci density along ... · 1 Patterns of recombination and MLH1 foci density along mouse chromosomes: modeling effects of interference and obligate
Heterozygous missense mutations in SMARCA2 cause ... · Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome Jeroen K. J. Van Houdt, Beata Anna Nowakowska,
Hypomagnesemia with Secondary Hypocalcemia due to a Missense
Clinical Studies Cancer Research MLH1 Founder Mutations ...rosenberglab.stanford.edu/papers/BorrasEtAl2010-CancerRes.pdf · Clinical Studies MLH1 Founder Mutations with Moderate Penetrance
Functional Analyses of Four CYP1A1 Missense Mutations
Toward Classification of BRCA1 Missense Variants Using a
The missense of smell: functional variability in the human
MLH1 Antibody - Cell Applications, Inc. · 2020. 2. 7. · MLH1 Antibody Cat. No. CP10170 Applications: Detected MW: Species & Reactivity: Isotype: WB, IP, IHC, ICC 85 kDa Human,
A missense mutation in SNRPE linked to non-syndromal
MLH1/PMS2 Expression Could Tell Classical NTRK Fusion in
Assessment of missense alterations in MLH1 and their ......Pethe, Miralem Mrkonjic, George Charames, Ken Kron, Jamie Rawson, Liyang Liu, Brian Li, Ted Chappell, Roula Raptis, Pinella
P53 Missense Mutation Cancer. Outline Disease related to p53 Role and regulation pathway Structure of p53 Missense mutation and consequences Experiment’s
A recurrent de novo missense mutation in causes
