Works matching IS 09143505 AND DT 2018 AND VI 58 AND IP 2

Results: 9

Interkinetic nuclear migration in the tracheal and esophageal epithelia of the mouse embryo: Possible implications for tracheo‐esophageal anomalies.

Published in:

Congenital Anomalies, 2018, v. 58, n. 2, p. 62, doi. 10.1111/cga.12241

By:

Kaneda, Ryo;
Saeki, Yuko;
Getachew, Dereje;
Matsumoto, Akihiro;
Furuya, Motohide;
Ogawa, Noriko;
Motoya, Tomoyuki;
Rafiq, Ashiq M.;
Jahan, Esrat;
Udagawa, Jun;
Hashimoto, Ryuju;
Otani, Hiroki

Publication type:

Article

Comment on “A prospective study on fetal posterior cranial fossa assessment for early detection of open spina bifida at 11–13 weeks” by Kose et al.

Published in:

Congenital Anomalies, 2018, v. 58, n. 2, p. 77, doi. 10.1111/cga.12265

By:

Lachmann, Robert

Publication type:

Article

Unilateral lung agenesis, aplasia or hypoplasia: Which one is it?

Published in:

Congenital Anomalies, 2018, v. 58, n. 2, p. 75, doi. 10.1111/cga.12239

By:

Nguyen, Khristopher M.;
Vala, Snehal;
Milla, Sarah S.;
Guglani, Lokesh

Publication type:

Article

Pentalogy of Cantrell in a monozygotic twin with a giant omphalocele firmly attached to the amniotic membrane: Successful prenatal diagnosis and cesarean delivery.

Published in:

Congenital Anomalies, 2018, v. 58, n. 2, p. 73, doi. 10.1111/cga.12237

By:

Kanasugi, Tomonobu;
Kikuchi, Akihiko;
Uesugi, Noriyuki;
Fukagawa, Daisuke;
Chida, Hideyuki;
Sasaki, Yuri;
Haba, Gen;
Isurugi, Chizuko;
Oyama, Rie;
Sugai, Tamotsu;
Sugiyama, Toru

Publication type:

Article

Announcement.

Published in:: Congenital Anomalies, 2018, v. 58, n. 2, p. 78, doi. 10.1111/cga.12274
Publication type:: Article

Issue Information.

Published in:: Congenital Anomalies, 2018, v. 58, n. 2, p. 45, doi. 10.1111/cga.12246
Publication type:: Article

Three‐dimensional models of the segmented human fetal brain generated by magnetic resonance imaging.

Published in:

Congenital Anomalies, 2018, v. 58, n. 2, p. 48, doi. 10.1111/cga.12229

By:

Yamaguchi, Yutaka;
Miyazaki, Reina;
Kamatani, Mikako;
Uwabe, Chigako;
Makishima, Haruyuki;
Nagai, Momoko;
Katsube, Motoki;
Yamamoto, Akira;
Imai, Hirohiko;
Kose, Katsumi;
Togashi, Kaori;
Yamada, Shigehito

Publication type:

Article

Congenital duodenal and multiple jejunal atresia with malrotation in a patient with Down syndrome.

Published in:

Congenital Anomalies, 2018, v. 58, n. 2, p. 71, doi. 10.1111/cga.12236

By:

Shironomae, Tsubasa;
Satomi, Miwa;
Kuwahara, Tsuyoshi;
Yasui, Yoshitomo;
Kohno, Miyuki

Publication type:

Article

Whole genome SNP genotyping in a family segregating developmental dysplasia of the hip detected runs of homozygosity on chromosomes 15q13.3 and 19p13.2.

Published in:

Congenital Anomalies, 2018, v. 58, n. 2, p. 56, doi. 10.1111/cga.12235

By:

Basit, Sulman;
Alharby, Essa;
Albalawi, Alia M.;
Khoshhal, Khalid I.

Publication type:

Article