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                             32 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Alan R. Clarke (ed): Transgenesis techniques — principles and protocols, 2nd edn. Theuring, Franz
 2002
 111 2 p. 229-230
 artikel
2 A life of Sir Francis Galton. From African exploration to the birth of eugenics Harper, Peter S.
 2002
 111 2 p. 225
 artikel
3 Androgen receptor CAG polymorphism and prostate cancer risk Mononen, Nina
 2002
 111 2 p. 166-171
 artikel
4 Androgen receptor CAG polymorphism and prostate cancer risk Mononen, Nina
 2002
 111 2 p. 166-171
 artikel
5 DNA hypermethylation: when tumour suppressor genes go silent Garinis, George A.
 2002
 111 2 p. 115-127
 artikel
6 DNA hypermethylation: when tumour suppressor genes go silent Garinis, George A.
 2002
 111 2 p. 115-127
 artikel
7 Evidence for a gene influencing heart rate on chromosome 4 among hypertensives Wilk, Jemma B.
 2002
 111 2 p. 207-213
 artikel
8 Evidence for a gene influencing heart rate on chromosome 4 among hypertensives Wilk, Jemma B.
 2002
 111 2 p. 207-213
 artikel
9 Evolution of a VNTR located within the promoter region of the thiopurine methyltransferase gene: inferences from population and sequence data Alves, Sandra
 2002
 111 2 p. 172-178
 artikel
10 Evolution of a VNTR located within the promoter region of the thiopurine methyltransferase gene: inferences from population and sequence data Alves, Sandra
 2002
 111 2 p. 172-178
 artikel
11 FOXP2: novel exons, splice variants, and CAG repeat length stability Bruce, Heather A.
 2002
 111 2 p. 136-144
 artikel
12 FOXP2: novel exons, splice variants, and CAG repeat length stability Bruce, Heather A.
 2002
 111 2 p. 136-144
 artikel
13 Functional characterization of a natural variant of luteinizing hormone Liao, W.
 2002
 111 2 p. 219-224
 artikel
14 Functional characterization of a natural variant of luteinizing hormone Liao, W.
 2002
 111 2 p. 219-224
 artikel
15 Functional characterization of the new human GABAA receptor mutation β3(R192H) Buhr, Andreas
 2002
 111 2 p. 154-160
 artikel
16 Functional characterization of the new human GABAA receptor mutation β3(R192H) Buhr, Andreas
 2002
 111 2 p. 154-160
 artikel
17 Human connexin26 (GJB2) deafness mutations affect the function of gap junction channels at different levels of protein expression. Thönnissen, Eva
 2002
 111 2 p. 190-197
 artikel
18 Human connexin26 (GJB2) deafness mutations affect the function of gap junction channels at different levels of protein expression. Thönnissen, Eva
 2002
 111 2 p. 190-197
 artikel
19 Major gene evidence after MTHFR-segregation analysis of serum homocysteine in families of patients undergoing coronary arteriography Jee, Sun
 2002
 111 2 p. 128-135
 artikel
20 Major gene evidence after MTHFR-segregation analysis of serum homocysteine in families of patients undergoing coronary arteriography Jee, Sun
 2002
 111 2 p. 128-135
 artikel
21 Megalencephalic leukoencephalopathy with subcortical cysts; a founder effect in Israeli patients and a higher than expected carrier rate among Libyan Jews Ben-Zeev, Bruria
 2002
 111 2 p. 214-218
 artikel
22 Megalencephalic leukoencephalopathy with subcortical cysts; a founder effect in Israeli patients and a higher than expected carrier rate among Libyan Jews Ben-Zeev, Bruria
 2002
 111 2 p. 214-218
 artikel
23 Organization of the human liver carnitine palmitoyltransferase 1 gene (CPT1A) and identification of novel mutations in hypoketotic hypoglycaemia Gobin, Stéphanie
 2002
 111 2 p. 179-189
 artikel
24 Organization of the human liver carnitine palmitoyltransferase 1 gene (CPT1A) and identification of novel mutations in hypoketotic hypoglycaemia Gobin, Stéphanie
 2002
 111 2 p. 179-189
 artikel
25 Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in Austria Janecke, Andreas R.
 2002
 111 2 p. 145-153
 artikel
26 Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in Austria Janecke, Andreas R.
 2002
 111 2 p. 145-153
 artikel
27 Psychosocial genetic counseling Evans, Christin L.
 2002
 111 2 p. 226
 artikel
28 Simopoulos AP, Pavlou KN (eds): Nutrition and fitness: Diet, genes, physical activity and health. World review of nutrition and dietetics, vol 89 Schickle, Darren
 2002
 111 2 p. 227-228
 artikel
29 SOX10 mutations in chronic intestinal pseudo-obstruction suggest a complex physiopathological mechanism Pingault, Véronique
 2002
 111 2 p. 198-206
 artikel
30 SOX10 mutations in chronic intestinal pseudo-obstruction suggest a complex physiopathological mechanism Pingault, Véronique
 2002
 111 2 p. 198-206
 artikel
31 Unexpectedly high prevalence of the mild form of propionic acidemia in Japan: presence of a common mutation and possible clinical implications Yorifuji, Tohru
 2002
 111 2 p. 161-165
 artikel
32 Unexpectedly high prevalence of the mild form of propionic acidemia in Japan: presence of a common mutation and possible clinical implications Yorifuji, Tohru
 2002
 111 2 p. 161-165
 artikel
                             32 gevonden resultaten
 
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