Works matching IS 09143505 AND DT 2017 AND VI 57 AND IP 3
Results: 7
Issue Information.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 3, p. 69, doi. 10.1111/cga.12183
- Publication type:
- Article
Variable presentation of Fraser syndrome in two fetuses and a novel mutation in FRAS1.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 3, p. 83, doi. 10.1111/cga.12188
- By:
- Publication type:
- Article
Patterns and risk factors of birth defects in rural areas of south-eastern Gabon.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 3, p. 79, doi. 10.1111/cga.12201
- By:
- Publication type:
- Article
Selective serotonin reuptake inhibitors and risk of major congenital anomalies for pregnancies in Japan: A nationwide birth cohort study of the Japan Environment and Children's Study.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 3, p. 72, doi. 10.1111/cga.12202
- By:
- Publication type:
- Article
Bilateral choanal atresia in an adult woman with pycnodysostosis.
- Published in:
- 2017
- By:
- Publication type:
- Other
Remnant cartilage in the middle ear.
- Published in:
- 2017
- By:
- Publication type:
- Other
A Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome with a KAT6B 10-base pair palindromic duplication: A recurrent mutation causing a severe phenotype mixed with genitopatellar syndrome.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 3, p. 86, doi. 10.1111/cga.12196
- By:
- Publication type:
- Article