Issue Information.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 2, p. 29, doi. 10.1111/cga.12296
- Publication type:
- Article
Works matching IS 09143505 AND DT 2019 AND VI 59 AND IP 2
Results: 7
1
2
17q21.32‐q22 Deletion in a girl with osteogenesis imperfecta, tricho‐dento‐osseous syndrome, and intellectual disability.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 2, p. 51, doi. 10.1111/cga.12292
- By:
- Publication type:
- Article
3
Novel mutation in EFCAB7 alters expression and interaction of Ellis–van Creveld ciliary proteins.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 2, p. 49, doi. 10.1111/cga.12291
- By:
- Publication type:
- Article
4
Rare urogenital anomaly variant with a separated didelphic uterus and ipsilateral renal agenesis without hemivagina: A case report.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 2, p. 47, doi. 10.1111/cga.12290
- By:
- Publication type:
- Article
5
Survival in double aneuploidy involving trisomy 18 and sex chromosome trisomy: A case report of a 27‐month‐old child and a review of the literature.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 2, p. 43, doi. 10.1111/cga.12287
- By:
- Publication type:
- Article
6
Effects of the Y‐chromosome and the dominant hemimelia mutation on the morphology of the mouse mandible.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 2, p. 32, doi. 10.1111/cga.12286
- By:
- Publication type:
- Article
7
Developmental toxicity of flucytosine following administration to pregnant rats at a specific time point of organogenesis.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 2, p. 39, doi. 10.1111/cga.12282
- By:
- Publication type:
- Article