TY  - GEN
AU  - Zhou,X P
AU  - Woodford-Richens,K
AU  - Lehtonen,R
AU  - Kurose,K
AU  - Aldred,M
AU  - Hampel,H
AU  - Launonen,V
AU  - Virta,S
AU  - Pilarski,R
AU  - Salovaara,R
AU  - Bodmer,W F
AU  - Conrad,B A
AU  - Dunlop,M
AU  - Hodgson,S V
AU  - Iwama,T
AU  - Järvinen,H
AU  - Kellokumpu,I
AU  - Kim,J C
AU  - Leggett,B
AU  - Markie,D
AU  - Mecklin,J P
AU  - Neale,K
AU  - Phillips,R
AU  - Piris,J
AU  - Rozen,P
AU  - Houlston,R S
AU  - Aaltonen,L A
AU  - Tomlinson,I P
AU  - Eng,C
TI  - Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes
SN  - 0002-9297
PY  - 2001///1018
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Bone Morphogenetic Protein Receptors, Type I
KW  - Colonic Neoplasms
KW  - complications
KW  - DNA Mutational Analysis
KW  - Genotype
KW  - Germ-Line Mutation
KW  - Hamartoma Syndrome, Multiple
KW  - Humans
KW  - Intestinal Polyps
KW  - Loss of Heterozygosity
KW  - Microsatellite Repeats
KW  - Phenotype
KW  - Protein Serine-Threonine Kinases
KW  - Receptors, Growth Factor
KW  - Receptors, Transforming Growth Factor beta
KW  - chemistry
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1086/323703
ER  -