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                             36 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Acknowledgement to Referees 2001 2001
 110 1 p. 107-110
 artikel
2 A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene Aung, Tin
 2001
 110 1 p. 52-56
 artikel
3 A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene Aung, Tin
 2001
 110 1 p. 52-56
 artikel
4 Authors response to: Critique of "Chromosome 17 and inducible nitric oxide synthase gene in human essential hypertension" by Rutherford et al. in Human Genetics published on-line September 2001 Griffiths, Lyn R.
 2001
 110 1 p. 100-103
 artikel
5 Authors response to: Critique of "Chromosome 17 and inducible nitric oxide synthase gene in human essential hypertension" by Rutherford et al. in Human Genetics published on-line September 2001 Griffiths, Lyn R.
 2001
 110 1 p. 100-103
 artikel
6 Critique of “Chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension” by Rutherford et al., Human Genetics, published online September 2001 Morris, Brian J.
 2001
 110 1 p. 98-99
 artikel
7 Cytogenetic mapping of a novel locus for type II Waardenburg syndrome Selicorni, Angelo
 2001
 110 1 p. 64-67
 artikel
8 Cytogenetic mapping of a novel locus for type II Waardenburg syndrome Selicorni, Angelo
 2001
 110 1 p. 64-67
 artikel
9 Dissecting the epidemiology of a trinucleotide repeat disease – example of FRDA in Finland Juvonen, Vesa
 2001
 110 1 p. 36-40
 artikel
10 Dissecting the epidemiology of a trinucleotide repeat disease – example of FRDA in Finland Juvonen, Vesa
 2001
 110 1 p. 36-40
 artikel
11 Familial idiopathic basal ganglia calcification (Fahr's disease) without neurological, cognitive and psychiatric symptoms is not linked to the IBGC1 locus on chromosome 14q Brodaty, Henry
 2001
 110 1 p. 8-14
 artikel
12 Familial idiopathic basal ganglia calcification (Fahr's disease) without neurological, cognitive and psychiatric symptoms is not linked to the IBGC1 locus on chromosome 14q Brodaty, Henry
 2001
 110 1 p. 8-14
 artikel
13 Fetal gender determination in early pregnancy through qualitative and quantitative analysis of fetal DNA in maternal serum Honda, Hiroshi
 2001
 110 1 p. 75-79
 artikel
14 Fetal gender determination in early pregnancy through qualitative and quantitative analysis of fetal DNA in maternal serum Honda, Hiroshi
 2001
 110 1 p. 75-79
 artikel
15 Genetic variations in the cholesteryl ester transfer protein gene and high density lipoprotein cholesterol levels in Taiwanese Chinese Hsu, Lung-An
 2001
 110 1 p. 57-63
 artikel
16 Genetic variations in the cholesteryl ester transfer protein gene and high density lipoprotein cholesterol levels in Taiwanese Chinese Hsu, Lung-An
 2001
 110 1 p. 57-63
 artikel
17 Investigation of the functional effect of monoamine oxidase polymorphisms in human brain Balciuniene, J.
 2001
 110 1 p. 1-7
 artikel
18 Investigation of the functional effect of monoamine oxidase polymorphisms in human brain Balciuniene, J.
 2001
 110 1 p. 1-7
 artikel
19 Joyce C. Harper, Joy D.A. Delhanty, Alan H. Handyside (eds): Preimplantation genetic diagnosis Flinter, Francis
 2001
 110 1 p. 105-106
 artikel
20 Laminin 5 mutations in junctional epidermolysis bullosa: molecular basis of Herlitz vs non-Herlitz phenotypes Nakano, Aoi
 2001
 110 1 p. 41-51
 artikel
21 Laminin 5 mutations in junctional epidermolysis bullosa: molecular basis of Herlitz vs non-Herlitz phenotypes Nakano, Aoi
 2001
 110 1 p. 41-51
 artikel
22 Linkage disequilibrium between GABRB3 gene and nonsyndromic familial cleft lip with or without cleft palate Scapoli, Luca
 2001
 110 1 p. 15-20
 artikel
23 Linkage disequilibrium between GABRB3 gene and nonsyndromic familial cleft lip with or without cleft palate Scapoli, Luca
 2001
 110 1 p. 15-20
 artikel
24 Mutations in human glycine N-methyltransferase give insights into its role in methionine metabolism Luka, Zigmund
 2001
 110 1 p. 68-74
 artikel
25 Mutations in human glycine N-methyltransferase give insights into its role in methionine metabolism Luka, Zigmund
 2001
 110 1 p. 68-74
 artikel
26 Paraoxonase gene Gln192Arg (Q192R) polymorphism is associated with coronary artery spasm Ito, Teruhiko
 2001
 110 1 p. 89-94
 artikel
27 Paraoxonase gene Gln192Arg (Q192R) polymorphism is associated with coronary artery spasm Ito, Teruhiko
 2001
 110 1 p. 89-94
 artikel
28 Rate of homologous chromosome bivalents in spermatocytes may predict completion of spermatogenesis in azoospermic men Yogev, Leah
 2001
 110 1 p. 30-35
 artikel
29 Rate of homologous chromosome bivalents in spermatocytes may predict completion of spermatogenesis in azoospermic men Yogev, Leah
 2001
 110 1 p. 30-35
 artikel
30 The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome Santer, René
 2001
 110 1 p. 21-29
 artikel
31 The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome Santer, René
 2001
 110 1 p. 21-29
 artikel
32 The USH1C 216G→A mutation and the 9-repeat VNTR(t,t) allele are in complete linkage disequilibrium in the Acadian population Savas, Sevtap
 2001
 110 1 p. 95-97
 artikel
33 The USH1C 216G→A mutation and the 9-repeat VNTR(t,t) allele are in complete linkage disequilibrium in the Acadian population Savas, Sevtap
 2001
 110 1 p. 95-97
 artikel
34 Three major lineages of Asian Y chromosomes: implications for the peopling of east and southeast Asia Tajima, Atsushi
 2001
 110 1 p. 80-88
 artikel
35 Three major lineages of Asian Y chromosomes: implications for the peopling of east and southeast Asia Tajima, Atsushi
 2001
 110 1 p. 80-88
 artikel
36 Ulrich R. Hengge, Beatrix Volc-Platzer (eds): The skin and gene therapy Happle, Rudolf
 2001
 110 1 p. 104
 artikel
                             36 gevonden resultaten
 
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