[HTML] cell.comFull View

[HTML][HTML] A restricted spectrum of mutations in the SMAD4 tumor-suppressor gene underlies Myhre syndrome

V Caputo, L Cianetti, M Niceta, C Carta, A Ciolfi… - The American Journal of …, 2012 - cell.com
Myhre syndrome is a developmental disorder characterized by reduced growth, generalized
muscular hypertrophy, facial dysmorphism, deafness, cognitive deficits, joint stiffness, and …
被引用次数：93 相关文章

[引用][C] A Restricted Spectrum of Mutations in the SMAD4 Tumor-Suppressor Gene Underlies Myhre Syndrome

V Caputo, L Cianetti, M Niceta, C Carta… - AMERICAN …, 2012 - art.torvergata.it
A Restricted Spectrum of Mutations in the SMAD4 Tumor-Suppressor Gene Underlies Myhre
Syndrome IRIS IRIS Home Sfoglia Macrotipologie & tipologie Autore Titolo Riviste Serie Settore …

A Restricted Spectrum of Mutations in the SMAD4 Tumor-Suppressor Gene Underlies Myhre Syndrome

V Caputo, L Cianetti, M Niceta, C Carta, A Ciolfi… - The American Journal of …, 2012 - infona.pl
Myhre syndrome is a developmental disorder characterized by reduced growth, generalized
muscular hypertrophy, facial dysmorphism, deafness, cognitive deficits, joint stiffness, and …

A restricted spectrum of mutations in the SMAD4 tumor-suppressor gene underlies Myhre syndrome.

V Caputo, L Cianetti, M Niceta, C Carta… - American Journal of …, 2012 - europepmc.org
Myhre syndrome is a developmental disorder characterized by reduced growth, generalized
muscular hypertrophy, facial dysmorphism, deafness, cognitive deficits, joint stiffness, and …

A restricted spectrum of mutations in the SMAD4 tumor-suppressor gene underlies Myhre syndrome

V Caputo, L Cianetti, M Niceta, C Carta… - … JOURNAL OF HUMAN …, 2012 - iris.unisa.it
Myhre syndrome is a developmental disorder characterized by reduced growth, generalized
muscular hypertrophy, facial dysmorphism, deafness, cognitive deficits, joint stiffness, and …

A restricted spectrum of mutations in the SMAD4 tumor-suppressor gene underlies myhre syndrome

V Caputo, L Cianetti, M Niceta, C Carta… - … JOURNAL OF HUMAN …, 2012 - iris.uniroma1.it
Myhre syndrome is a developmental disorder characterized by reduced growth, generalized
muscular hypertrophy, facial dysmorphism, deafness, cognitive deficits, joint stiffness, and …
[PDF] core.ac.uk

[PDF][PDF] Viviana Caputo, Luciano Cianetti, Marcello Niceta, Claudio Carta, Andrea Ciolfi, Gianfranco Bocchinfuso, 2 Eugenio Carrani, 3 Maria Lisa Dentici, 4 Elisa …

L Stella, M Silengo, B Dallapiccola… - The American Journal of …, 2012 - core.ac.uk
Myhre syndrome is a developmental disorder characterized by reduced growth, generalized
muscular hypertrophy, facial dysmorphism, deafness, cognitive deficits, joint stiffness, and …
[PDF] cyberleninka.org

[PDF][PDF] Viviana Caputo, Luciano Cianetti, Marcello Niceta, Claudio Carta, Andrea Ciolfi, Gianfranco Bocchinfuso, 2 Eugenio Carrani, 3 Maria Lisa Dentici, 4 Elisa …

L Stella, M Silengo, B Dallapiccola… - The American Journal …, 2012 - cyberleninka.org
Myhre syndrome is a developmental disorder characterized by reduced growth, generalized
muscular hypertrophy, facial dysmorphism, deafness, cognitive deficits, joint stiffness, and …

A restricted spectrum of mutations in the SMAD4 tumor-suppressor gene underlies Myhre syndrome

V Caputo, L Cianetti, M Niceta… - … journal of human …, 2012 - pubmed.ncbi.nlm.nih.gov
Myhre syndrome is a developmental disorder characterized by reduced growth, generalized
muscular hypertrophy, facial dysmorphism, deafness, cognitive deficits, joint stiffness, and …

[引用][C] A Restricted Spectrum of Mutations in the SMAD4 Tumor-Suppressor Gene Underlies Myhre Syndrome

V CAPUTO, L CIANETTI, L GARAVELLI… - American journal of …, 2012 - pascal-francis.inist.fr
A Restricted Spectrum of Mutations in the SMAD4 Tumor-Suppressor Gene Underlies
Myhre Syndrome CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic …