Works matching IS 09143505 AND DT 2022 AND VI 62 AND IP 1

Results: 10

Issue Information.

Published in:: Congenital Anomalies, 2022, v. 62, n. 1, p. 1, doi. 10.1111/cga.12423
Publication type:: Article

Announcement.

Published in:: Congenital Anomalies, 2022, v. 62, n. 1, p. 49, doi. 10.1111/cga.12455
Publication type:: Article

The Japanese Teratology Society 61st Annual Meeting.

Published in:: Congenital Anomalies, 2022, v. 62, n. 1, p. A1, doi. 10.1111/cga.12453
Publication type:: Article

Involvement of homeobox transcription factor Mohawk in palatogenesis.

Published in:

Congenital Anomalies, 2022, v. 62, n. 1, p. 27, doi. 10.1111/cga.12451

By:

Adachi, Yuka;
Higuchi, Aina;
Wakai, Eri;
Shiromizu, Takashi;
Koiwa, Junko;
Nishimura, Yuhei

Publication type:

Article

Identification of a novel mutant allele of LIM homeobox transcription factor 1 alpha (dreher) in mice.

Published in:: Congenital Anomalies, 2022, v. 62, n. 1, p. 18, doi. 10.1111/cga.12450
Publication type:: Article

Periconceptional folic acid intake and disturbing factors: A single‐center study in Japan.

Published in:

Congenital Anomalies, 2022, v. 62, n. 1, p. 42, doi. 10.1111/cga.12449

By:

Kamura, Shunsuke;
Sasaki, Aiko;
Ogawa, Kohei;
Kato, Kiyoko;
Sago, Haruhiko

Publication type:

Article

A Japanese family with a heterozygous novel mutation in the Indian hedgehog gene exhibiting a broad spectrum of clinical features and radiological findings.

Published in:

Congenital Anomalies, 2022, v. 62, n. 1, p. 47, doi. 10.1111/cga.12445

By:

Onuki, Takanori;
Shibata, Nao;
Hiroshima, Shota;
Sawano, Kentaro;
Nagasaki, Keisuke

Publication type:

Article

Changes in the birth prevalence of orofacial clefts in Japan: Has the birth prevalence of orofacial clefts been affected by improved accuracy of prenatal diagnosis?

Published in:

Congenital Anomalies, 2022, v. 62, n. 1, p. 11, doi. 10.1111/cga.12444

By:

Natsume, Nagato;
Furukawa, Hiroo;
Niimi, Teruyuki;
Takeuchi, Kazuo;
Yoshida, Waka;
Sakuma, Chisato;
Imura, Hideto;
Fujiwara, Kumiko;
Akashi, Junko;
Hayami, Kayo;
Natsume, Nagana

Publication type:

Article

The association between the congenital heart diseases and congenital anomalies of the kidney and the urinary tract in nonsyndromic children.

Published in:

Congenital Anomalies, 2022, v. 62, n. 1, p. 4, doi. 10.1111/cga.12443

By:

Alp, Esma Keleş;
Dönmez, Muhammet İrfan;
Alp, Hayrullah;
Elmacı, Ahmet Midhat

Publication type:

Article

Parenchymal calcification is associated with the neurological prognosis in patients with congenital rubella syndrome.

Published in:

Congenital Anomalies, 2022, v. 62, n. 1, p. 38, doi. 10.1111/cga.12442

By:

Namiki, Takahiro;
Takano, Chika;
Aoki, Ryoji;
Trinh, Quang Duy;
Morioka, Ichiro;
Hayakawa, Satoshi

Publication type:

Article