Announcement.
- Published in:
- 2017
- Publication type:
- Other
Works matching IS 09143505 AND DT 2017 AND VI 57 AND IP 4
Results: 8
1
2
Issue Information.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 4, p. 93, doi. 10.1111/cga.12184
- Publication type:
- Article
3
Possible genes responsible for developmental delay observed in patients with rare 2q23q24 microdeletion syndrome: Literature review and description of an additional patient.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 4, p. 109, doi. 10.1111/cga.12205
- By:
- Publication type:
- Article
4
Changeability of the fully methylated status of the 15q11.2 region in induced pluripotent stem cells derived from a patient with Prader-Willi syndrome.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 4, p. 96, doi. 10.1111/cga.12206
- By:
- Publication type:
- Article
5
Hearing impairment in a female infant with interstitial deletion of 2q24.1q24.3.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 4, p. 118, doi. 10.1111/cga.12207
- By:
- Publication type:
- Article
6
Co-occurrence of bronchial atresia and intrapulmonary sequestration in divergent lobes.
- Published in:
- 2017
- By:
- Publication type:
- Other
7
Regional difference in sulcal infolding progression correlated with cerebral cortical expansion in cynomolgus monkey fetuses.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 4, p. 114, doi. 10.1111/cga.12209
- By:
- Publication type:
- Article
8
Surgical strategy for Apert syndrome: Retrospective study of developmental quotient and three-dimensional computerized tomography.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 4, p. 104, doi. 10.1111/cga.12222
- By:
- Publication type:
- Article