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C. Van Broeckhoven

Veröffentlichungen von C. Van Broeckhoven zu Broeckhoven, C. ->
weitere Veröffentlichungen von C. Van Broeckhoven:
Reply to — Alzheimer's disease and the family effect (1994)
Unique sequence homology in the pericentromeric regions of the long arms of chromosomes 13 and 21 (1992)
Genomic organisation of the spinocerebellar ataxia type 7 (SCA7) gene responsible for autosomal dominant cerebellar ataxia with retinal degeneration (1999)
Hyperargininemia: The rat as a model for the human disease and the comparative response to enzyme replacement therapy with free arginase and arginase-loaded erythrocytes in vivo (1984)
Hereditäre Neuralgische Amyotrophie (HNA): Klinische und molekulargenetische Befunde (1998)
Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving field (1999)
Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family (2000)
Primary and secondary structure of the 18 S ribosomal RNA of the insect species Tenebrio molitor (1988)
Localization of a Gene Responsible for Nonspecific Mental Retardation (MRX9) to the Pericentromeric Region of the X Chromosome (1993)
The pericentromeric 21 DNA marker pGSM21 (D21S13) contains an expressed HTF island (1990)
Presenile Alzheimer dementia characterized by amyloid angiopathy and large amyloid core type senile plaques in the APP 692Ala→Gly mutation (1998)
Cloning and sequence analysis of the gene encoding human lymphocyte prolyl endopeptidase (1994)
Measurement of arginine transport in human erythrocytes using their intrinsic arginase activity: implications for the treatment of familial hyperargininemia (1982)
Cloning and Characterization of a 135- to 500-kb Region of Homology on the Long Arm of Human Chromosome 21 (1994)
Refinement of the locus for autosomal dominant cerebellar ataxia type II to chromosome 3p21.1–14.1 (1997)
Veröffentlichungen zu Broeckhoven, C.
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1
van Duijn, C., Van Broeckhoven, C. Reply to — Alzheimer's disease and the family effect
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 8, No. 2 (1994), p. 115-115
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1994
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2
Camp, G., Vandenberghe, A., ... An informative MspI polymorphism detected at the D21S16 locus
in: Human genetics , ISSN 1432-1203, Vol. 85 (1. 1990), p. 140-140
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1990
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3
Nelles, L., Broeckhoven, C., ... Location of the hidden break in large subunit ribosomal RNA of Artemia salina
in: Naturwissenschaften , ISSN 1432-1904, Vol. 71 (12. 1984), p. 634-635
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1984
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4
Michalík, A., Del-Favero, J., ... Genomic organisation of the spinocerebellar ataxia type 7 (SCA7) gene responsible for autosomal dominant cerebellar ataxia with retinal degeneration
in: Human genetics , ISSN 1432-1203, Vol. 105 (5. 1999), p. 410-417
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1999
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5
Adriaenssens, K., Karcher, D., ... Hyperargininemia: The rat as a model for the human disease and the comparative response to enzyme replacement therapy with free arginase and arginase-loaded erythrocytes in vivo
in: International Journal of Biochemistry, in: International Journal of Biochemistry . - Amsterdam : Elsevier, ISSN 0020-711X, ZDB-ID 2168113-2 Vol. 16, No. 7 (1984), p. 779-786
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1984
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6
Stögbauer, F.. Hereditäre Neuralgische Amyotrophie (HNA): Klinische und molekulargenetische Befunde
In: Fortschritte der Neurologie, Psychiatrie. - Stuttgart [u.a.] : Thieme Vol. 66, No. 01 (1. 1998), p. 10-14
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1998
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7
Camp, G., Backhovens, H., ... Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndrome
in: Human genetics , ISSN 1432-1203, Vol. 87 (6. 1991), p. 649-653
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1991
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8
Uhlhaas, S., Bakker, E., ... A rare MspI RFLP of the DMD probe p20 (DXS269)
in: Human genetics , ISSN 1432-1203, Vol. 89 (1. 1992), p. 122-122
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1992
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9
Segers, K., Singh, S. K., ... Immunoreactivity for p53 and mdm2 and the detection of p53 mutations in human malignant mesothelioma
in: Virchows Archiv , ISSN 1432-2307, Vol. 427 (4. 1995), p. 431-436
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1995
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10
Nelis, E., Timmerman, V., ... Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving field
in: Neurogenetics , ISSN 1364-6753, Vol. 2 (3. 1999), p. 137-148
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1999
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11
Leonardis, L., Zidar, J., ... Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family
in: Pflügers Archiv , ISSN 1432-2013, Vol. 439 (7. 2000), p. r208
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2000
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12
Hendriks, L., De Baere, R., ... Primary and secondary structure of the 18 S ribosomal RNA of the insect species Tenebrio molitor
in: FEBS Letters, in: FEBS Letters . - Amsterdam : Elsevier, ISSN 0014-5793, ZDB-ID 1460391-3 Vol. 232, No. 1 (1988), p. 115-120
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1988
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13
Van Camp, G., Cruts, M., ... Unique sequence homology in the pericentromeric regions of the long arms of chromosomes 13 and 21
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 12, No. 1 (1992), p. 158-160
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1992
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14
Willems, P., Vits, L., ... Localization of a Gene Responsible for Nonspecific Mental Retardation (MRX9) to the Pericentromeric Region of the X Chromosome
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 18, No. 2 (1993), p. 290-294
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1993
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15
Gosset, P., Crété, N., ... A High-resolution map of 1.6 Mb in the Down syndrome region: a new map between D21S55 and ETS2
in: Mammalian genome , ISSN 1432-1777, Vol. 6 (2. 1995), p. 127-130
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1995
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16
Beuten, Joke, Mangelschots, Kathelijne, ... Molecular study of chromosome 15 in 22 patients with Angelman syndrome
in: Human genetics , ISSN 1432-1203, Vol. 90 (5. 1993), p. 489-495
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1993
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17
Vanhoof, G., Goossens, F., ... Cloning and sequence analysis of the gene encoding human lymphocyte prolyl endopeptidase
in: Gene, in: Gene . - Amsterdam : Elsevier, ISSN 0378-1119, ZDB-ID 1491012-3 Vol. 149, No. 2 (1994), p. 363-366
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1994
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18
Van Broeckhoven, C.L., Adriaenssens, K.M., ... Measurement of arginine transport in human erythrocytes using their intrinsic arginase activity: implications for the treatment of familial hyperargininemia
in: Clinica Chimica Acta, in: Clinica Chimica Acta . - Amsterdam : Elsevier, ISSN 0009-8981, ZDB-ID 1499920-1 Vol. 126, No. 3 (1982), p. 209-216
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1982
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19
Stinissen, P., Van Hul, W., ... The pericentromeric 21 DNA marker pGSM21 (D21S13) contains an expressed HTF island
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 7, No. 1 (1990), p. 119-122
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1990
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20
Cras, P., van Harskamp, F., ... Presenile Alzheimer dementia characterized by amyloid angiopathy and large amyloid core type senile plaques in the APP 692Ala→Gly mutation
in: Acta neuropathologica , ISSN 1432-0533, Vol. 96 (3. 1998), p. 253-260
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1998