Works matching IS 09143505 AND DT 2018 AND VI 58 AND IP 4

Results: 11

Announcement.

Published in:: Congenital Anomalies, 2018, v. 58, n. 4, p. 148, doi. 10.1111/cga.12289
Publication type:: Article

Association between a common missense variant in LOXL3 gene and the risk of non‐syndromic cleft palate.

Published in:

Congenital Anomalies, 2018, v. 58, n. 4, p. 136, doi. 10.1111/cga.12288

By:

Khan, Mohammad Faisal J.;
Little, Julian;
Mossey, Peter A.;
Steegers‐Theunissen, Régine P. M.;
Bonsi, Martina;
Bassi Andreasi, Rita;
Rubini, Michele

Publication type:

Article

Prevalence of orofacial clefts and risks for nonsyndromic cleft lip with or without cleft palate in newborns at a university hospital from West Mexico.

Published in:

Congenital Anomalies, 2018, v. 58, n. 4, p. 117, doi. 10.1111/cga.12276

By:

Corona‐Rivera, Jorge Román;
Bobadilla‐Morales, Lucina;
Corona‐Rivera, Alfredo;
Peña‐Padilla, Christian;
Olvera‐Molina, Sandra;
Orozco‐Martín, Miriam A.;
García‐Cruz, Diana;
Ríos‐Flores, Izabel M.;
Gómez‐Rodríguez, Brian Gabriel;
Rivas‐Soto, Gemma;
Pérez‐Molina, J. Jesús

Publication type:

Article

Association of single nucleotide polymorphisms in WNT genes with the risk of nonsyndromic cleft lip with or without cleft palate.

Published in:

Congenital Anomalies, 2018, v. 58, n. 4, p. 130, doi. 10.1111/cga.12271

By:

Rafighdoost, Houshang;
Hashemi, Mohammad;
Asadi, Hossein;
Bahari, Gholamreza

Publication type:

Article

International volunteer surgical project for cleft lip/cleft palate in Laos.

Published in:

Congenital Anomalies, 2018, v. 58, n. 4, p. 147, doi. 10.1111/cga.12263

By:

Joob, Beuy;
Wiwanitkit, Viroj

Publication type:

Article

Association of MEOX2 polymorphism with nonsyndromic cleft palate only in a Vietnamese population.

Published in:

Congenital Anomalies, 2018, v. 58, n. 4, p. 124, doi. 10.1111/cga.12259

By:

Tran, Duy L.;
Imura, Hideto;
Mori, Akihiro;
Suzuki, Satoshi;
Niimi, Teruyuki;
Ono, Maya;
Sakuma, Chisato;
Nakahara, Shinichi;
Nguyen, Tham T. H.;
Pham, Phuong T.;
Hoang, Viet;
Tran, Van T. T.;
Nguyen, Minh D.;
Natsume, Nagato

Publication type:

Article

Novel AMER1 frameshift mutation in a girl with osteopathia striata with cranial sclerosis.

Published in:

Congenital Anomalies, 2018, v. 58, n. 4, p. 145, doi. 10.1111/cga.12258

By:

Enomoto, Yumi;
Tsurusaki, Yoshinori;
Harada, Noriaki;
Aida, Noriko;
Kurosawa, Kenji

Publication type:

Article

Outcomes of an international volunteer surgical project for patients with cleft lip and/or cleft palate: A mission in developing Laos.

Published in:

Congenital Anomalies, 2018, v. 58, n. 4, p. 112, doi. 10.1111/cga.12255

By:

Goto, Takahiro;
Nishihara, Kazuhide;
Kataoka, Keiichi;
Goto, Shinpei;
Maruyama, Tessho;
Sunakawa, Hajime;
Natsume, Nagato;
Arasaki, Akira

Publication type:

Article

Novel A178P mutation in SLC16A2 in a patient with Allan‐Herndon‐Dudley syndrome.

Published in:

Congenital Anomalies, 2018, v. 58, n. 4, p. 143, doi. 10.1111/cga.12251

By:

Yamamoto, Toshiyuki;
Lu, Yongping;
Nakamura, Ryoko;
Shimojima, Keiko;
Kira, Ryutaro

Publication type:

Article

Issue Information.

Published in:: Congenital Anomalies, 2018, v. 58, n. 4, p. 109, doi. 10.1111/cga.12248
Publication type:: Article

Retroperitoneal gastric duplication mimicking a prenatal adrenal cyst.

Published in:

Congenital Anomalies, 2018, v. 58, n. 4, p. 141, doi. 10.1111/cga.12244

By:

Castillo‐Fernández, Aurora Lucía;
Vázquez‐Rueda, Fernando;
Cañete, Mª Dolores;
Caballero‐Villarraso, Javier

Publication type:

Article