Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes

X P Zhou, K Woodford-Richens, R Lehtonen, K Kurose, M Aldred, H Hampel, V Launonen, S Virta, R Pilarski, R Salovaara, W F Bodmer, B A Conrad, M Dunlop, S V Hodgson, T Iwama, H Jarvinen, I Kellokumpu, J C Kim, B Leggett, D MarkieJ P Mecklin, K Neale, R Phillips, J Piris, P Rozen, R S Houlston, L A Aaltonen, I P M Tomlinson, C Eng

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalAmerican Journal of Human Genetics
Volume69
Pages (from-to)704-711
Number of pages8
ISSN0002-9297
Publication statusPublished - 2001
MoE publication typeA1 Journal article-refereed

Fields of Science

  • PEUTZ-JEGHERS-SYNDROME
  • PTEN MUTATION
  • ZONANA-SYNDROME
  • GENE
  • DISEASE
  • DELETION
  • SPECTRUM
  • 10Q22-23
  • CANCER
  • KINASE

Cite this

Zhou, X P ; Woodford-Richens, K ; Lehtonen, R ; Kurose, K ; Aldred, M ; Hampel, H ; Launonen, V ; Virta, S ; Pilarski, R ; Salovaara, R ; Bodmer, W F ; Conrad, B A ; Dunlop, M ; Hodgson, S V ; Iwama, T ; Jarvinen, H ; Kellokumpu, I ; Kim, J C ; Leggett, B ; Markie, D ; Mecklin, J P ; Neale, K ; Phillips, R ; Piris, J ; Rozen, P ; Houlston, R S ; Aaltonen, L A ; Tomlinson, I P M ; Eng, C . / Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes. In: American Journal of Human Genetics. 2001 ; Vol. 69. pp. 704-711.
@article{c53605cc5ab04ab782b648289bac7e3b,
title = "Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes",
keywords = "PEUTZ-JEGHERS-SYNDROME, PTEN MUTATION, ZONANA-SYNDROME, GENE, DISEASE, DELETION, SPECTRUM, 10Q22-23, CANCER, KINASE",
author = "Zhou, {X P} and K Woodford-Richens and R Lehtonen and K Kurose and M Aldred and H Hampel and V Launonen and S Virta and R Pilarski and R Salovaara and Bodmer, {W F} and Conrad, {B A} and M Dunlop and Hodgson, {S V} and T Iwama and H Jarvinen and I Kellokumpu and Kim, {J C} and B Leggett and D Markie and Mecklin, {J P} and K Neale and R Phillips and J Piris and P Rozen and Houlston, {R S} and Aaltonen, {L A} and Tomlinson, {I P M} and C Eng",
year = "2001",
language = "English",
volume = "69",
pages = "704--711",
journal = "American Journal of Human Genetics",
issn = "0002-9297",
publisher = "Cell Press",

}

Zhou, XP, Woodford-Richens, K, Lehtonen, R, Kurose, K, Aldred, M, Hampel, H, Launonen, V, Virta, S, Pilarski, R, Salovaara, R, Bodmer, WF, Conrad, BA, Dunlop, M, Hodgson, SV, Iwama, T, Jarvinen, H, Kellokumpu, I, Kim, JC, Leggett, B, Markie, D, Mecklin, JP, Neale, K, Phillips, R, Piris, J, Rozen, P, Houlston, RS, Aaltonen, LA, Tomlinson, IPM & Eng, C 2001, 'Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes', American Journal of Human Genetics, vol. 69, pp. 704-711.

Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes. / Zhou, X P ; Woodford-Richens, K ; Lehtonen, R ; Kurose, K ; Aldred, M ; Hampel, H ; Launonen, V ; Virta, S ; Pilarski, R ; Salovaara, R ; Bodmer, W F ; Conrad, B A ; Dunlop, M ; Hodgson, S V ; Iwama, T ; Jarvinen, H ; Kellokumpu, I ; Kim, J C ; Leggett, B ; Markie, D ; Mecklin, J P ; Neale, K ; Phillips, R ; Piris, J ; Rozen, P ; Houlston, R S ; Aaltonen, L A ; Tomlinson, I P M ; Eng, C .

In: American Journal of Human Genetics, Vol. 69, 2001, p. 704-711.

Research output: Contribution to journalArticleScientificpeer-review

TY - JOUR

T1 - Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes

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 - Jarvinen, 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 M

AU - Eng, C

PY - 2001

Y1 - 2001

KW - PEUTZ-JEGHERS-SYNDROME

KW - PTEN MUTATION

KW - ZONANA-SYNDROME

KW - GENE

KW - DISEASE

KW - DELETION

KW - SPECTRUM

KW - 10Q22-23

KW - CANCER

KW - KINASE

M3 - Article

VL - 69

SP - 704

EP - 711

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

SN - 0002-9297

ER -