Works matching IS 24721727 AND DT 2020 AND VI 112 AND IP 10

Results: 9

Issue Information.

Published in:: Birth Defects Research, 2020, v. 112, n. 10, p. 699, doi. 10.1002/bdr2.1757
Publication type:: Article

Compound craniosynostosis, intellectual disability, and Noonan‐like facial dysmorphism associated with 7q32.3‐q35 deletion.

Published in:

Birth Defects Research, 2020, v. 112, n. 10, p. 740, doi. 10.1002/bdr2.1744

By:

Bukowska‐Olech, Ewelina;
Dmitrzak‐Węglarz, Monika;
Larysz, Dawid;
Wojciechowicz, Bartosz;
Simon, Dorota;
Walczak‐Sztulpa, Joanna;
Jamsheer, Aleksander

Publication type:

Article

Cover Image.

Published in:: Birth Defects Research, 2020, v. 112, n. 10, p. 1, doi. 10.1002/bdr2.1756
Publication type:: Article

Swimming toward solutions: Using fish and frogs as models for understanding RASopathies.

Published in:

Birth Defects Research, 2020, v. 112, n. 10, p. 749, doi. 10.1002/bdr2.1707

By:

Patterson, Victoria L.;
Burdine, Rebecca D.

Publication type:

Article

Introduction to the special issue on "RASopathies: Misregulation of signaling".

Published in:

Birth Defects Research, 2020, v. 112, n. 10, p. 703, doi. 10.1002/bdr2.1701

By:

Watanabe, Michiko

Publication type:

Article

Noonan syndrome on the African Continent.

Published in:

Birth Defects Research, 2020, v. 112, n. 10, p. 718, doi. 10.1002/bdr2.1675

By:

Tekendo‐Ngongang, Cedrik;
Kruszka, Paul

Publication type:

Article

GTP hydrolysis is modulated by Arg34 in the RASopathy‐associated KRAS<sup>P34R</sup>.

Published in:

Birth Defects Research, 2020, v. 112, n. 10, p. 708, doi. 10.1002/bdr2.1647

By:

Bera, Asim K.;
Lu, Jia;
Lu, Chunya;
Li, Lianbo;
Gondi, Sudershan;
Yan, Wei;
Nelson, Andrew;
Zhang, Goujun;
Westover, Kenneth D.

Publication type:

Article

Atypical cardiac defects in patients with RASopathies: Updated data on CARNET study.

Published in:

Birth Defects Research, 2020, v. 112, n. 10, p. 725, doi. 10.1002/bdr2.1670

By:

Calcagni, Giulio;
Gagliostro, Giulia;
Limongelli, Giuseppe;
Unolt, Marta;
De Luca, Enrica;
Digilio, Maria C.;
Baban, Anwar;
Albanese, Sonia B.;
Ferrero, Giovanni B.;
Baldassarre, Giuseppina;
Agnoletti, Gabriella;
Banaudi, Elena;
Marek, Jan;
Kaski, Juan P.;
Tuo, Giulia;
Marasini, Maurizio;
Cairello, Francesca;
Madrigali, Andrea;
Pacileo, Giuseppe;
Russo, Maria G.

Publication type:

Article

Noonan syndrome with multiple Giant cell lesions, management and treatment with surgery and interferon alpha‐2a therapy: Case report.

Published in:

Birth Defects Research, 2020, v. 112, n. 10, p. 732, doi. 10.1002/bdr2.1659

By:

Rodríguez, Fernando Adrián;
Castellón, Loreto;
Moreno, Regina;
Paez, Eduardo;
Aracena Álvarez, Mariana Inés

Publication type:

Article