PMID- 10528862
OWN - NLM
STAT- MEDLINE
DCOM- 19991119
LR  - 20190503
IS  - 0022-2593 (Print)
IS  - 0022-2593 (Linking)
VI  - 36
IP  - 10
DP  - 1999 Oct
TI  - A missense mutation in both hMSH2 and APC in an Ashkenazi Jewish HNPCC kindred:
      implications for clinical screening.
PG  - 790-3
FAU - Yuan, Z Q
AU  - Yuan ZQ
FAU - Wong, N
AU  - Wong N
FAU - Foulkes, W D
AU  - Foulkes WD
FAU - Alpert, L
AU  - Alpert L
FAU - Manganaro, F
AU  - Manganaro F
FAU - Andreutti-Zaugg, C
AU  - Andreutti-Zaugg C
FAU - Iggo, R
AU  - Iggo R
FAU - Anthony, K
AU  - Anthony K
FAU - Hsieh, E
AU  - Hsieh E
FAU - Redston, M
AU  - Redston M
FAU - Pinsky, L
AU  - Pinsky L
FAU - Trifiro, M
AU  - Trifiro M
FAU - Gordon, P H
AU  - Gordon PH
FAU - Lasko, D
AU  - Lasko D
LA  - eng
PT  - Letter
PT  - Research Support, Non-U.S. Gov't
PL  - England
TA  - J Med Genet
JT  - Journal of medical genetics
JID - 2985087R
RN  - 0 (Adaptor Proteins, Signal Transducing)
RN  - 0 (Adenomatous Polyposis Coli Protein)
RN  - 0 (Carrier Proteins)
RN  - 0 (Cytoskeletal Proteins)
RN  - 0 (DNA-Binding Proteins)
RN  - 0 (MLH1 protein, human)
RN  - 0 (Neoplasm Proteins)
RN  - 0 (Nuclear Proteins)
RN  - 0 (Proto-Oncogene Proteins)
RN  - EC 3.6.1.3 (MSH2 protein, human)
RN  - EC 3.6.1.3 (MutL Protein Homolog 1)
RN  - EC 3.6.1.3 (MutS Homolog 2 Protein)
SB  - IM
MH  - Adaptor Proteins, Signal Transducing
MH  - Adenomatous Polyposis Coli Protein
MH  - Carrier Proteins
MH  - Colorectal Neoplasms, Hereditary Nonpolyposis/*genetics
MH  - Cytoskeletal Proteins/*genetics
MH  - *DNA-Binding Proteins
MH  - Female
MH  - Genetic Predisposition to Disease
MH  - Humans
MH  - Jews
MH  - Male
MH  - Microsatellite Repeats
MH  - MutL Protein Homolog 1
MH  - MutS Homolog 2 Protein
MH  - *Mutation, Missense
MH  - Neoplasm Proteins/genetics
MH  - Nuclear Proteins
MH  - Nucleic Acid Conformation
MH  - Nucleic Acid Hybridization
MH  - Pedigree
MH  - Proto-Oncogene Proteins/*genetics
MH  - Risk Factors
PMC - PMC3622028
EDAT- 1999/10/21 00:00
MHDA- 1999/10/21 00:01
CRDT- 1999/10/21 00:00
PHST- 1999/10/21 00:00 [pubmed]
PHST- 1999/10/21 00:01 [medline]
PHST- 1999/10/21 00:00 [entrez]
AID - 10.1136/jmg.36.10.792 [doi]
PST - ppublish
SO  - J Med Genet. 1999 Oct;36(10):790-3. doi: 10.1136/jmg.36.10.792.