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Works matching IS 09143505 AND DT 2018 AND VI 58 AND IP 6

Results: 8

1

Reviewers.

Published in:: Congenital Anomalies, 2018, v. 58, n. 6, p. 198, doi. 10.1111/cga.12315
Publication type:: Article

2

Abstracts.

Published in:: Congenital Anomalies, 2018, v. 58, n. 6, p. A1, doi. 10.1111/cga.12314
Publication type:: Article

3

Announcement.

Published in:: Congenital Anomalies, 2018, v. 58, n. 6, p. 199, doi. 10.1111/cga.12313
Publication type:: Article

4

58th Annual Meeting of the Japanese Teratology Society: Congenital anomalies as variants.

Published in:

Congenital Anomalies, 2018, v. 58, n. 6, p. 186, doi. 10.1111/cga.12310

By:

Numabe, Hironao

Publication type:

Article

5

Evaluation of a patient with classical Ehlers‐Danlos syndrome due to a 9q34 duplication affecting COL5A1.

Published in:

Congenital Anomalies, 2018, v. 58, n. 6, p. 191, doi. 10.1111/cga.12277

By:

Kuroda, Yukiko;
Ohashi, Ikuko;
Naruto, Takuya;
Ida, Kazumi;
Enomoto, Yumi;
Saito, Toshiyuki;
Nagai, Jun‐ichi;
Kurosawa, Kenji

Publication type:

Article

6

Novel SYNGAP1 variant in a patient with intellectual disability and distinctive dysmorphisms.

Published in:

Congenital Anomalies, 2018, v. 58, n. 6, p. 188, doi. 10.1111/cga.12273

By:

Kimura, Yuichi;
Akahira‐Azuma, Moe;
Harada, Noriaki;
Enomoto, Yumi;
Tsurusaki, Yoshinori;
Kurosawa, Kenji

Publication type:

Article

7

Issue Information.

Published in:: Congenital Anomalies, 2018, v. 58, n. 6, p. 183, doi. 10.1111/cga.12250
Publication type:: Article

8

Familial campomelic dysplasia due to maternal germinal mosaicism.

Published in:

Congenital Anomalies, 2018, v. 58, n. 6, p. 194, doi. 10.1111/cga.12279

By:

Higeta, Daisuke;
Yamaguchi, Rie;
Takagi, Takeshi;
Nishimura, Gen;
Sameshima, Kiyoko;
Saito, Kayoko;
Minegishi, Takashi

Publication type:

Article