| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes
|
Rozenblum, Ester
|
|
2001
|
110 |
2 |
p. 111-121
|
artikel
|
| 2 |
A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes
|
Rozenblum, Ester
|
|
2001
|
110 |
2 |
p. 111-121
|
artikel
|
| 3 |
C.R. Scriver, A.L. Beaudet, W.S. Sly, D. Valle (eds.), B. Childs, K.W. Kinzler, B. Vogelstein (associate eds.): Molecular and metabolic bases of inherited disease, 8th edition
|
Harper, Peter S.
|
|
2002
|
110 |
2 |
p. 205-206
|
artikel
|
| 4 |
Effectiveness of computational methods in haplotype prediction
|
Xu, Chun-Fang
|
|
2001
|
110 |
2 |
p. 148-156
|
artikel
|
| 5 |
Effectiveness of computational methods in haplotype prediction
|
Xu, Chun-Fang
|
|
2001
|
110 |
2 |
p. 148-156
|
artikel
|
| 6 |
Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene
|
Seri, Marco
|
|
2001
|
110 |
2 |
p. 182-186
|
artikel
|
| 7 |
Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene
|
Seri, Marco
|
|
2001
|
110 |
2 |
p. 182-186
|
artikel
|
| 8 |
Evidence of a founder effect and refinement of the hereditary neuralgic amyotrophy (HNA) locus on 17q25 in American families
|
Watts, Giles D.
|
|
2001
|
110 |
2 |
p. 166-172
|
artikel
|
| 9 |
Evidence of a founder effect and refinement of the hereditary neuralgic amyotrophy (HNA) locus on 17q25 in American families
|
Watts, Giles D.
|
|
2001
|
110 |
2 |
p. 166-172
|
artikel
|
| 10 |
Evidence of multiple causal sites affecting weight in the IGF2-INS-TH region of human chromosome 11
|
Gu, Dongfeng
|
|
2002
|
110 |
2 |
p. 173-181
|
artikel
|
| 11 |
Evidence of multiple causal sites affecting weight in the IGF2-INS-TH region of human chromosome 11
|
Gu, Dongfeng
|
|
2002
|
110 |
2 |
p. 173-181
|
artikel
|
| 12 |
Genetics in medicine (Sixth Edition)
|
Murray, Alexandra J.
|
|
2002
|
110 |
2 |
p. 203-204
|
artikel
|
| 13 |
Identification, genomic organization, chromosomal mapping and mutation analysis of the human INV gene, the ortholog of a murine gene implicated in left-right axis development and biliary atresia
|
Schön, Patric
|
|
2001
|
110 |
2 |
p. 157-165
|
artikel
|
| 14 |
Identification, genomic organization, chromosomal mapping and mutation analysis of the human INV gene, the ortholog of a murine gene implicated in left-right axis development and biliary atresia
|
Schön, Patric
|
|
2001
|
110 |
2 |
p. 157-165
|
artikel
|
| 15 |
Linkage analysis identifies the thyroglobulin gene region as a major locus for familial congenital hypothyroidism
|
Ahlbom, Bodil
|
|
2002
|
110 |
2 |
p. 145-147
|
artikel
|
| 16 |
Linkage analysis identifies the thyroglobulin gene region as a major locus for familial congenital hypothyroidism
|
Ahlbom, Bodil
|
|
2002
|
110 |
2 |
p. 145-147
|
artikel
|
| 17 |
Polymorphic GGC repeats in the androgen receptor gene are associated with hereditary and sporadic prostate cancer risk
|
Chang, Bao-li
|
|
2002
|
110 |
2 |
p. 122-129
|
artikel
|
| 18 |
Polymorphic GGC repeats in the androgen receptor gene are associated with hereditary and sporadic prostate cancer risk
|
Chang, Bao-li
|
|
2002
|
110 |
2 |
p. 122-129
|
artikel
|
| 19 |
Pyruvate dehydrogenase E3 binding protein deficiency
|
Brown, Ruth M.
|
|
2002
|
110 |
2 |
p. 187-191
|
artikel
|
| 20 |
Pyruvate dehydrogenase E3 binding protein deficiency
|
Brown, Ruth M.
|
|
2002
|
110 |
2 |
p. 187-191
|
artikel
|
| 21 |
Relaxation of imprinted expression of ZAC and HYMAI in a patient with transient neonatal diabetes mellitus
|
Mackay, D.
|
|
2002
|
110 |
2 |
p. 139-144
|
artikel
|
| 22 |
Relaxation of imprinted expression of ZAC and HYMAI in a patient with transient neonatal diabetes mellitus
|
Mackay, D.
|
|
2002
|
110 |
2 |
p. 139-144
|
artikel
|
| 23 |
Susceptibility gene for non-obstructive azoospermia located near HLA-DR and -DQ loci in the HLA class II region
|
Tsujimura, Akira
|
|
2002
|
110 |
2 |
p. 192-197
|
artikel
|
| 24 |
Susceptibility gene for non-obstructive azoospermia located near HLA-DR and -DQ loci in the HLA class II region
|
Tsujimura, Akira
|
|
2002
|
110 |
2 |
p. 192-197
|
artikel
|
| 25 |
The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J
|
Brown, Michael D.
|
|
2002
|
110 |
2 |
p. 130-138
|
artikel
|
| 26 |
The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J
|
Brown, Michael D.
|
|
2002
|
110 |
2 |
p. 130-138
|
artikel
|
| 27 |
Y-chromosomal evidence for a strong reduction in male population size of Yakuts
|
Pakendorf, Brigitte
|
|
2002
|
110 |
2 |
p. 198-200
|
artikel
|
| 28 |
Y-chromosomal evidence for a strong reduction in male population size of Yakuts
|
Pakendorf, Brigitte
|
|
2002
|
110 |
2 |
p. 198-200
|
artikel
|
| 29 |
ZNT4 gene is not responsible for acrodermatitis enteropathica in Japanese families
|
Nakano, Aoi
|
|
2002
|
110 |
2 |
p. 201-202
|
artikel
|
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