Works matching IS 09143505 AND DT 2019 AND VI 59 AND IP 3

Results: 9

Announcement.

Published in:: Congenital Anomalies, 2019, v. 59, n. 3, p. 104, doi. 10.1111/cga.12338
Publication type:: Article

Molecular mechanisms underlying the models of neurodevelopmental disorders in maternal immune activation relevant to the placenta.

Published in:

Congenital Anomalies, 2019, v. 59, n. 3, p. 81, doi. 10.1111/cga.12323

By:

Tsukada, Tsuyoshi;
Shimada, Hiroki;
Sakata‐Haga, Hiromi;
Iizuka, Hideaki;
Hatta, Toshihisa

Publication type:

Article

Developmental mutant mouse models for external genitalia formation.

Published in:

Congenital Anomalies, 2019, v. 59, n. 3, p. 74, doi. 10.1111/cga.12319

By:

Hashimoto, Daiki;
Hyuga, Taiju;
Acebedo, Alvin R.;
Alcantara, Mellissa C.;
Suzuki, Kentaro;
Yamada, Gen

Publication type:

Article

Congenital eye anomalies: More mosaic than thought?

Published in:

Congenital Anomalies, 2019, v. 59, n. 3, p. 56, doi. 10.1111/cga.12304

By:

Ohuchi, Hideyo;
Sato, Keita;
Habuta, Munenori;
Fujita, Hirofumi;
Bando, Tetsuya

Publication type:

Article

Identification and association of recurrent ALOXE3 mutation with non‐bullous congenital ichthyosiform erythroderma in two ethnically distinct Pakistani families.

Published in:

Congenital Anomalies, 2019, v. 59, n. 3, p. 93, doi. 10.1111/cga.12303

By:

Rahman, Simeen Ber;
Mir, Asif;
Ahmad, Nafees;
Haider, Syed Husnain;
Malik, Salman Akbar;
Nasir, Muhammad

Publication type:

Article

Potentially effective method for fetal gender determination by noninvasive prenatal testing for X‐linked disease.

Published in:

Congenital Anomalies, 2019, v. 59, n. 3, p. 88, doi. 10.1111/cga.12302

By:

Noda, Yoshiteru;
Kato, Takema;
Kato, Asuka;
Nishizawa, Haruki;
Miyazaki, Jun;
Ito, Mayuko;
Terasawa, Sumire;
Sekiya, Takao;
Fujii, Takuma;
Kurahashi, Hiroki

Publication type:

Article

Long‐term natural history of an adult patient with distal 22q11.2 deletion from low copy repeat‐D to E.

Published in:

Congenital Anomalies, 2019, v. 59, n. 3, p. 102, doi. 10.1111/cga.12301

By:

Matsuo, Mari;
Yamamoto, Toshiyuki;
Saito, Kayoko

Publication type:

Article

Issue Information.

Published in:: Congenital Anomalies, 2019, v. 59, n. 3, p. 53, doi. 10.1111/cga.12297
Publication type:: Article

Novel compound heterozygous and homozygous variants of laminin subunit β3 gene underlie non‐Herlitz junctional epidermolysis bullosa in two paternal half‐brothers from Saudi Arabia.

Published in:

Congenital Anomalies, 2019, v. 59, n. 3, p. 99, doi. 10.1111/cga.12294

By:

Al‐Zahrani, Hams S.;
Al‐Tala, Saeed;
Mohamoud, Hussein S. A.;
Al‐Shehri, Bandar A.;
Al‐Fadhel, Saeed;
Al‐Qurashi, Ali;
Al‐Bishri, Ahmad;
Al‐Aama, Jumana Y.;
Kang, Changsoo;
Betz, Regina C.;
Jelani, Musharraf

Publication type:

Article