Found: 8
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Hair anomalies as a sign of mitochondrial disease.
- Published in:
- European Journal of Pediatrics, 2003, v. 162, n. 7/8, p. 459, doi. 10.1007/s00431-003-1228-5
- By:
- Publication type:
- Article
Mental retardation, peculiar facial dysmorphism and HbH inclusions in a 4-year-old boy.
- Published in:
- 2002
- By:
- Publication type:
- journal article
Anthropometric characteristics of newborns with Prader–Willi syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 10, p. 2067, doi. 10.1002/ajmg.a.61304
- By:
- Publication type:
- Article
MIND THE GAP - TOWARDS THE ELIMINATION OF OPEN ASSEMBLY CONFIGURATION IN SEGMENTAL RETAINING WALLS.
- Published in:
- Journal of the South African Institution of Civil Engineering, 2018, v. 26, n. 7, p. 67
- By:
- Publication type:
- Article
In-vitro fertilisation and intra-uterine growth retardation.
- Published in:
- 1990
- By:
- Publication type:
- Letter
Dihydropteridine reductase deficiency in man: From biology to treatment.
- Published in:
- Medicinal Research Reviews, 2004, v. 24, n. 2, p. 127, doi. 10.1002/med.10055
- By:
- Publication type:
- Article
POLG mutations and Alpers syndrome.
- Published in:
- Annals of Neurology, 2005, v. 57, n. 6, p. 921
- By:
- Publication type:
- Article
Obituary for Prof. Alberto Ponzone.
- Published in:
- 2022
- By:
- Publication type:
- Obituary