Works matching IS 09143505 AND DT 2017 AND VI 57 AND IP 2

Results: 9

Miller-Dieker Syndrome with unbalanced translocation 45, X, psu dic(17;Y)(p13;p11.32) detected by fluorescence in situ hybridization and G-banding analysis using high resolution banding technique.

Published in:

Congenital Anomalies, 2017, v. 57, n. 2, p. 61, doi. 10.1111/cga.12193

By:

Mishima, Takashi;
Watari, Michiko;
Iwaki, Yutaka;
Nagai, Takumi;
Kawamata-Nakamura, Miho;
Kobayashi, Yukako;
Fujieda, Satoko;
Oikawa, Mamoru;
Takahashi, Nobuhiro;
Keira, Mitsuaki;
Yoshida, Hiroshi;
Tonoki, Hidefumi

Publication type:

Article

Late-presenting congenital diaphragmatic hernia in a child with TMEM70 deficiency.

Published in:

Congenital Anomalies, 2017, v. 57, n. 2, p. 64, doi. 10.1111/cga.12194

By:

Sarajlija, Adrijan;
Magner, Martin;
Djordjevic, Maja;
Kecman, Bozica;
Grujic, Blagoje;
Tesarova, Marketa;
Minic, Predrag

Publication type:

Article

Discordant ventriculo-arterial connections, or 'transposition', are not necessarily an essential part of isomerism.

Published in:

Congenital Anomalies, 2017, v. 57, n. 2, p. 66, doi. 10.1111/cga.12195

By:

Loomba, Rohit S.;
Anderson, Robert H.

Publication type:

Article

Magnetic resonance imaging based correlation analysis between calcarine sulcus development and isolated fetal ventriculomegaly.

Published in:

Congenital Anomalies, 2017, v. 57, n. 2, p. 52, doi. 10.1111/cga.12197

By:

Li, Hehong;
Liang, Huiying;
Wu, Huiying

Publication type:

Article

Locus on chromosome 16 is significantly associated with increased tendency to lose pups in females of the RR/Sgn inbred mouse strain.

Published in:

Congenital Anomalies, 2017, v. 57, n. 2, p. 57, doi. 10.1111/cga.12199

By:

Suto, Jun-ichi

Publication type:

Article

Proposal for supplemental intake of folic acid to reduce the risk of neural tube defects.

Published in:: 2017
Publication type:: Other

Announcement.

Published in:: 2017
Publication type:: Other

Issue Information.

Published in:: Congenital Anomalies, 2017, v. 57, n. 2, p. 41, doi. 10.1111/cga.12182
Publication type:: Article

Novel homozygous sequence variants in the GDF5 gene underlie acromesomelic dysplasia type-grebe in consanguineous families.

Published in:

Congenital Anomalies, 2017, v. 57, n. 2, p. 45, doi. 10.1111/cga.12187

By:

Umair, Muhammad;
Rafique, Afzal;
Ullah, Asmat;
Ahmad, Farooq;
Ali, Raja Hussain;
Nasir, Abdul;
Ansar, Muhammad;
Ahmad, Wasim

Publication type:

Article