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  2. Details for: Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis.
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Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis. [electronic resource]

By:
  • Martignetti, John A
Contributor(s):
  • Tian, Lifeng
  • Li, Dong
  • Ramirez, Maria Celeste M
  • Camacho-Vanegas, Olga
  • Camacho, Sandra Catalina
  • Guo, Yiran
  • Zand, Dina J
  • Bernstein, Audrey M
  • Masur, Sandra K
  • Kim, Cecilia E
  • Otieno, Frederick G
  • Hou, Cuiping
  • Abdel-Magid, Nada
  • Tweddale, Ben
  • Metry, Denise
  • Fournet, Jean-Christophe
  • Papp, Eniko
  • McPherson, Elizabeth W
  • Zabel, Carrie
  • Vaksmann, Guy
  • Morisot, Cyril
  • Keating, Brendan
  • Sleiman, Patrick M
  • Cleveland, Jeffrey A
  • Everman, David B
  • Zackai, Elaine
  • Hakonarson, Hakon
Producer: 20140109Description: 1001-7 p. digitalISSN:
  • 1537-6605
Subject(s):
  • Amino Acid Sequence
  • Base Sequence
  • Female
  • Genes, Dominant
  • Genetic Association Studies
  • Humans
  • Male
  • Mutation, Missense
  • Myofibromatosis -- congenital
  • Pedigree
  • Receptor, Notch3
  • Receptor, Platelet-Derived Growth Factor beta -- genetics
  • Receptors, Notch -- genetics
  • Sequence Analysis, DNA
Online resources:
  • Available from publisher's website
In: American journal of human genetics vol. 92
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis.

APA

Martignetti J. A., Tian L., Li D., Ramirez M. C. M., Camacho-Vanegas O., Camacho S. C., Guo Y., Zand D. J., Bernstein A. M., Masur S. K., Kim C. E., Otieno F. G., Hou C., Abdel-Magid N., Tweddale B., Metry D., Fournet J., Papp E., McPherson E. W., Zabel C., Vaksmann G., Morisot C., Keating B., Sleiman P. M., Cleveland J. A., Everman D. B., Zackai E. & Hakonarson H. (20140109). Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis. : American journal of human genetics.

Chicago

Martignetti John A, Tian Lifeng, Li Dong, Ramirez Maria Celeste M, Camacho-Vanegas Olga, Camacho Sandra Catalina, Guo Yiran, Zand Dina J, Bernstein Audrey M, Masur Sandra K, Kim Cecilia E, Otieno Frederick G, Hou Cuiping, Abdel-Magid Nada, Tweddale Ben, Metry Denise, Fournet Jean-Christophe, Papp Eniko, McPherson Elizabeth W, Zabel Carrie, Vaksmann Guy, Morisot Cyril, Keating Brendan, Sleiman Patrick M, Cleveland Jeffrey A, Everman David B, Zackai Elaine and Hakonarson Hakon. 20140109. Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis. : American journal of human genetics.

Harvard

Martignetti J. A., Tian L., Li D., Ramirez M. C. M., Camacho-Vanegas O., Camacho S. C., Guo Y., Zand D. J., Bernstein A. M., Masur S. K., Kim C. E., Otieno F. G., Hou C., Abdel-Magid N., Tweddale B., Metry D., Fournet J., Papp E., McPherson E. W., Zabel C., Vaksmann G., Morisot C., Keating B., Sleiman P. M., Cleveland J. A., Everman D. B., Zackai E. and Hakonarson H. (20140109). Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis. : American journal of human genetics.

MLA

Martignetti John A, Tian Lifeng, Li Dong, Ramirez Maria Celeste M, Camacho-Vanegas Olga, Camacho Sandra Catalina, Guo Yiran, Zand Dina J, Bernstein Audrey M, Masur Sandra K, Kim Cecilia E, Otieno Frederick G, Hou Cuiping, Abdel-Magid Nada, Tweddale Ben, Metry Denise, Fournet Jean-Christophe, Papp Eniko, McPherson Elizabeth W, Zabel Carrie, Vaksmann Guy, Morisot Cyril, Keating Brendan, Sleiman Patrick M, Cleveland Jeffrey A, Everman David B, Zackai Elaine and Hakonarson Hakon. Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis. : American journal of human genetics. 20140109.

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