Works matching IS 09143505 AND DT 2015 AND VI 55 AND IP 3

Results: 13

Severe respiratory distress at birth caused by a hairy polyp of the Eustachian tube: Transoral endoscopy-guided treatment.

Published in:

Congenital Anomalies, 2015, v. 55, n. 3, p. 158, doi. 10.1111/cga.12100

By:

Cantarella, Giovanna;
Gaffuri, Michele;
Pugni, Lorenza;
Pignataro, Lorenzo;
Mosca, Fabio

Publication type:

Article

Characteristics of 2p15-p16.1 microdeletion syndrome: Review and description of two additional patients.

Published in:

Congenital Anomalies, 2015, v. 55, n. 3, p. 125, doi. 10.1111/cga.12112

By:

Shimojima, Keiko;
Okamoto, Nobuhiko;
Yamamoto, Toshiyuki

Publication type:

Article

Novel compound heterozygous mutations in DYNC2H1 in a patient with severe short-rib polydactyly syndrome type III phenotype.

Published in:

Congenital Anomalies, 2015, v. 55, n. 3, p. 155, doi. 10.1111/cga.12098

By:

Okamoto, Toshio;
Nagaya, Ken;
Kawata, Yumi;
Asai, Hiroko;
Tsuchida, Etsushi;
Nohara, Fumikatsu;
Okajima, Kazuki;
Azuma, Hiroshi

Publication type:

Article

Epigenetic alterations in sperm associated with male infertility.

Published in:

Congenital Anomalies, 2015, v. 55, n. 3, p. 133, doi. 10.1111/cga.12113

By:

Kitamura, Akane;
Miyauchi, Naoko;
Hamada, Hirotaka;
Hiura, Hitoshi;
Chiba, Hatsune;
Okae, Hiroaki;
Sato, Akiko;
John, Rosalind M.;
Arima, Takahiro

Publication type:

Article

The mystery of post-axial polydactyly in Renaissance paintings.

Published in:

Congenital Anomalies, 2015, v. 55, n. 3, p. 171, doi. 10.1111/cga.12115

By:

Coralli, Alessia;
Perciaccante, Antonio

Publication type:

Article

Issue Information.

Published in:: Congenital Anomalies, 2015, v. 55, n. 3, p. i, doi. 10.1111/cga.12084
Publication type:: Article

Prenatal findings of holoprosencephaly.

Published in:

Congenital Anomalies, 2015, v. 55, n. 3, p. 161, doi. 10.1111/cga.12103

By:

Hayashi, Yuko;
Suzumori, Nobuhiro;
Sugiura, Tokio;
Sugiura-Ogasawara, Mayumi

Publication type:

Article

Fetal cytomegalovirus infection manifesting as transient pancytopenia.

Published in:

Congenital Anomalies, 2015, v. 55, n. 3, p. 164, doi. 10.1111/cga.12104

By:

Kiyokoba, Ryo;
Hidaka, Nobuhiro;
Sakata, Yukiyo;
Hachisuga, Kazuhisa;
Fukushima, Kotaro;
Kato, Kiyoko

Publication type:

Article

Adult phenotype of Russell-Silver syndrome: A molecular support for Barker-Brenner's theory.

Published in:

Congenital Anomalies, 2015, v. 55, n. 3, p. 167, doi. 10.1111/cga.12105

By:

Takenouchi, Toshiki;
Awazu, Midori;
Eggermann, Thomas;
Kosaki, Kenjiro

Publication type:

Article

No increases in the rate of undescended testis in Hungary during the last 50 years: A population-based study.

Published in:

Congenital Anomalies, 2015, v. 55, n. 3, p. 145, doi. 10.1111/cga.12106

By:

Mavrogenis, Stelios;
Ács, Nándor;
Czeizel, Andrew E.

Publication type:

Article

Causes of the failure and the revision methods for congenital scoliosis due to hemivertebra.

Published in:

Congenital Anomalies, 2015, v. 55, n. 3, p. 150, doi. 10.1111/cga.12107

By:

Shi, Zhicai;
Li, Quan;
Cai, Bin;
Yu, Baoqing;
Feng, Yuan;
Wu, Jibin;
Li, Ming;
Ran, Bo

Publication type:

Article

Caudate lobe of the liver as the only content of the umbilical cord hernia.

Published in:

Congenital Anomalies, 2015, v. 55, n. 3, p. 170, doi. 10.1111/cga.12108

By:

Boybeyi, Özlem;
Ozmen, Ismail;
Dere Gunal, Yasemin;
Aslan, Mustafa Kemal;
Aliefendioglu, Didem

Publication type:

Article

Announcement.

Published in:: Congenital Anomalies, 2015, v. 55, n. 3, p. J3, doi. 10.1111/cga.12120
Publication type:: Article