Found: 11
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Familial Optic Atrophy with Sex-Influenced Severity.
- Published in:
- Ophthalmologica, 1986, v. 192, n. 1, p. 28, doi. 10.1159/000309608
- By:
- Publication type:
- Article
Congenital Obstruction of the Lacrimal Passages in Five Consecutive Generations.
- Published in:
- Ophthalmologica, 1980, v. 181, n. 3/4, p. 129, doi. 10.1159/000309040
- By:
- Publication type:
- Article
Dystrophie congénitale héréditaire de la cornée associée à des anomalies extraoculaires diverses.
- Published in:
- Ophthalmologica, 1975, v. 171, n. 6, p. 410, doi. 10.1159/000307564
- By:
- Publication type:
- Article
Prenatal diagnosis of thalassemia: the viewpoint of patients.
- Published in:
- 1988
- By:
- Publication type:
- journal article
Treatment of Infantile Spasms with Sodium Dipropylacetic Acid.
- Published in:
- Developmental Medicine & Child Neurology, 1981, v. 23, n. 5, p. 454, doi. 10.1111/j.1469-8749.1981.tb02018.x
- By:
- Publication type:
- Article
Familial centronuclear myopathy.
- Published in:
- Acta Neurologica Scandinavica, 1980, v. 62, n. 1, p. 33, doi. 10.1111/j.1600-0404.1980.tb03001.x
- By:
- Publication type:
- Article
Should All Children Receive Two Measles Vaccinations?
- Published in:
- 1993
- By:
- Publication type:
- Letter
Eight new mutations of the phenylalanine hydroxylase gene in Italian patients with hyperphenylalaninemia.
- Published in:
- Human Mutation, 1998, v. 11, n. 3, p. 240, doi. 10.1002/(SICI)1098-1004(1998)11:3<240::AID-HUMU9>3.0.CO;2-L
- By:
- Publication type:
- Article
Single base pair deletions in exons 39 and 42 of the COL4A5 gene in Alport syndrome.
- Published in:
- Human Molecular Genetics, 1994, v. 3, n. 1, p. 201
- By:
- Publication type:
- Article
Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis of hyperphenyl-alaninemia in Southern Europe.
- Published in:
- Human Molecular Genetics, 1993, v. 2, n. 10, p. 1703
- By:
- Publication type:
- Article
Ocular manifestations in a family with probably X-linked cataracts.
- Published in:
- Clinical Genetics, 1981, v. 20, n. 4, p. 243, doi. 10.1111/j.1399-0004.1981.tb01028.x
- By:
- Publication type:
- Article