108 results on '"Went Ln"'
Search Results
2. Epidemiological and clinical aspects of hereditary cerebral hemorrhage in Dutch families
3. Incidence of Abnormal Hæmoglobins in Jamaica
4. Leber hereditary optic neuropathy (LHON): a mitochondrial disease with unresolved complexities.
5. Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia.
6. Hereditary spastic dystonia with Leber's hereditary optic neuropathy: neuropathological findings.
7. Human tritanopia associated with a third amino acid substitution in the blue-sensitive visual pigment.
8. X linked progressive cone dystrophy with specific attention to carrier detection.
9. Late onset dominant cone dystrophy with early blue cone involvement.
10. Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsin.
11. Hereditary spastic dystonia: a new mitochondrial encephalopathy? Putaminal necrosis as a diagnostic sign.
12. Dominant cone dystrophy starting with blue cone involvement.
13. Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene.
14. Color matching and foveal densitometry in patients and carriers of an X-linked progressive cone dystrophy.
15. Ocular melanoma in families with dysplastic nevus syndrome.
16. Tumour spectrum in the FAMMM syndrome.
17. Genetic linkage studies in Huntington's chorea.
18. Increment spectral sensitivity of hemizygotes and heterozygotes for different classes of colour vision.
19. Ages of death of children with Huntington's chorea and of their affected parents.
20. Huntington's Chorea in the Netherlands. The problem of genetic heterogeneity.
21. Genetic aspects of erythropoietic protoporphyria.
22. Haemoglobin Lepore Boston and elliptocytosis in a family of Indonesian-German ancestry.
23. An unusual form of spinal muscular atrophy with mental retardation occurring in an inbred population.
24. Epidemiological and clinical aspects of hereditary cerebral hemorrhage in Dutch families.
25. Frequencies of different types of colour vision defects in the Netherlands.
26. Linkage investigations in two families with hereditary ataxia.
27. The genetics of tritan disturbances.
28. Primary choroidal and cutaneous melanomas, bilateral choroidal melanomas, and familial occurrence of melanomas.
29. Leber's optic neuropathy I. Clinical studies.
30. Genetics of colour vision.
31. Familial hypokalemic periodic paralysis. 50-year follow-up of a large family.
32. Genetic linkage between erythrokeratodermia variabilis and Rh locus.
33. Comparative colour vision and other ophthalmological studies in three families with dominant inherited juvenile optic atrophy.
34. [A breakthrough in research on Huntington's chorea].
35. New test for the detection of tritan defects evaluated in two surveys.
36. X-linked incomplete achromatopsia with more than one class of functional cones.
37. Ophthalmologic and genetic study of a family with nyctalopia and myopia.
38. Parental transmission in Huntington's disease.
39. A search for associations between genetical polymorphic systems and physical, biochemical and Haematological variables.
40. Familial cerebral amyloid angiopathy presenting as recurrent cerebral haemorrhage.
41. Farnsworth-Munsell 100-hue results in a series of patients with long-standing therapeutic carotenaemia.
42. Color matching in autosomal dominant tritan defect.
43. Binding of Protoporphyrin to hemoglobin in red blood cells of patients with erythropoietic protoporphyria.
44. Leber's optic neuropathy II. Fluorescein angiographic studies.
45. [Familial cerebral hemorrhage as a result of cerebral amyloid angiopathy].
46. Studies in dominant optic atrophy.
47. Colour vision, ophthalmological and linkage studies in a pedigree with a tritan defect.
48. Haemoglobin A2-NYU in the Netherlands. Incidence of delta-chain variants in human populations.
49. [Familial dysplastic nevus syndrome in the Netherlands; various clinical and genetic aspects].
50. Familial benign hypercalcaemia (FBH; McK. No. 14598, 1983): linkage studies in a large Dutch family.
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