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Works matching IS 09143505 AND DT 2022 AND VI 62 AND IP 2

Results: 5

1

Cohesinopathy presenting with microtia, facial palsy, and hearing loss caused by STAG1 pathogenic variant.

Published in:

Congenital Anomalies, 2022, v. 62, n. 2, p. 82, doi. 10.1111/cga.12454

By:

Funato, Michinori;
Uehara, Tomoko;
Okada, Yuki;
Kaneko, Hideo;
Kosaki, Kenjiro

Publication type:

Article

2

Potential role of viral infections in miscarriage and insights into the underlying molecular mechanisms.

Published in:

Congenital Anomalies, 2022, v. 62, n. 2, p. 54, doi. 10.1111/cga.12458

By:

Heydarifard, Zahra;
Zadheidar, Sevrin;
Yavarian, Jila;
Shatizadeh Malekshahi, Somayeh;
Kalantari, Shirin;
Mokhtari‐Azad, Talat;
Shafiei‐Jandaghi, Nazanin‐Zahra

Publication type:

Article

3

Analysis of triptan use during pregnancy in Japan: A case series.

Published in:

Congenital Anomalies, 2022, v. 62, n. 2, p. 78, doi. 10.1111/cga.12456

By:

Yamaguchi, Yuko;
Yamada, Takahiro;
Goto, Mikako;
Kawasaki, Hidenori;
Wada, Takahito;
Ikeda‐Sakai, Yasuko;
Saito, Yoshiyuki;
Hayashi, Masahiro;
Tanaka, Shiro;
Takahashi, Ryosuke;
Nakayama, Takeo;
Murashima, Atsuko;
Kosugi, Shinji

Publication type:

Article

4

Issue Information.

Published in:: Congenital Anomalies, 2022, v. 62, n. 2, p. 51, doi. 10.1111/cga.12424
Publication type:: Article

5

Two new patients with focal dermal hypoplasia: A novel PORCN variant and insights on the diagnostic considerations.

Published in:

Congenital Anomalies, 2022, v. 62, n. 2, p. 68, doi. 10.1111/cga.12457

By:

Elhossini, Rasha Moheb;
Abdel‐Hamid, Mohamed S.;
Ashaat, Engy;
Otaify, Ghada A.;
Dawoud, Heba;
Elshimy, Khalid;
El Ruby, Mona;
Aglan, Mona

Publication type:

Article