| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP)
|
Gu, C. Charles
|
|
2007
|
121 |
5 |
p. 577-590
|
artikel
|
| 2 |
An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP)
|
Gu, C. Charles
|
|
|
121 |
5 |
p. 577-590
|
artikel
|
| 3 |
A novel locus for distal motor neuron degeneration maps to chromosome 7q34-q36
|
Gopinath, Sumana
|
|
|
121 |
5 |
p. 559-564
|
artikel
|
| 4 |
A novel locus for distal motor neuron degeneration maps to chromosome 7q34-q36
|
Gopinath, Sumana
|
|
2007
|
121 |
5 |
p. 559-564
|
artikel
|
| 5 |
Anthony H. Futerman, Ari Zimran: Gaucher Disease
|
Wraith, Ed
|
|
2007
|
121 |
5 |
p. 643-644
|
artikel
|
| 6 |
A recurrent mutation in type II collagen gene causes Legg-Calvé-Perthes disease in a Japanese family
|
Miyamoto, Yoshinari
|
|
|
121 |
5 |
p. 625-629
|
artikel
|
| 7 |
A recurrent mutation in type II collagen gene causes Legg-Calvé-Perthes disease in a Japanese family
|
Miyamoto, Yoshinari
|
|
2007
|
121 |
5 |
p. 625-629
|
artikel
|
| 8 |
Association of ALOX5AP with ischemic stroke: a population-based case-control study
|
Kaushal, Ritesh
|
|
2007
|
121 |
5 |
p. 601-607
|
artikel
|
| 9 |
Association of ALOX5AP with ischemic stroke: a population-based case-control study
|
Kaushal, Ritesh
|
|
|
121 |
5 |
p. 601-607
|
artikel
|
| 10 |
A strong association between human earwax-type and apocrine colostrum secretion from the mammary gland
|
Miura, Kiyonori
|
|
2007
|
121 |
5 |
p. 631-633
|
artikel
|
| 11 |
A strong association between human earwax-type and apocrine colostrum secretion from the mammary gland
|
Miura, Kiyonori
|
|
|
121 |
5 |
p. 631-633
|
artikel
|
| 12 |
Genetic admixture, adipocytokines, and adiposity in Black Americans: the Health, Aging, and Body Composition study
|
Wassel Fyr, Christina L.
|
|
|
121 |
5 |
p. 615-624
|
artikel
|
| 13 |
Genetic admixture, adipocytokines, and adiposity in Black Americans: the Health, Aging, and Body Composition study
|
Wassel Fyr, Christina L.
|
|
2007
|
121 |
5 |
p. 615-624
|
artikel
|
| 14 |
Genetic ancestry, population sub-structure, and cardiovascular disease-related traits among African-American participants in the CARDIA Study
|
Reiner, Alexander P.
|
|
2007
|
121 |
5 |
p. 565-575
|
artikel
|
| 15 |
Genetic ancestry, population sub-structure, and cardiovascular disease-related traits among African-American participants in the CARDIA Study
|
Reiner, Alexander P.
|
|
|
121 |
5 |
p. 565-575
|
artikel
|
| 16 |
Genetic markers for glutamic acid decarboxylase do not predict insulin-dependent diabetes mellitus in pairs of affected siblings
|
Rambrand, Tina
|
|
2007
|
121 |
5 |
p. 653
|
artikel
|
| 17 |
Genetic polymorphisms in transforming growth factor beta-1 (TGFB1) and childhood asthma and atopy
|
Li, Huiling
|
|
2007
|
121 |
5 |
p. 529-538
|
artikel
|
| 18 |
Genetic polymorphisms in transforming growth factor beta-1 (TGFB1) and childhood asthma and atopy
|
Li, Huiling
|
|
|
121 |
5 |
p. 529-538
|
artikel
|
| 19 |
J. R. Lupski and P.T. Stankiewicz: Genomic disorders: the genomic basis of disease
|
Shaw-Smith, Charles
|
|
2007
|
121 |
5 |
p. 639-640
|
artikel
|
| 20 |
J. R. Lupski and P.T. Stankiewicz: Genomic disorders: the genomic basis of disease
|
Shaw-Smith, Charles
|
|
|
121 |
5 |
p. 639-640
|
artikel
|
| 21 |
Kenneth Lyons Jones (ed): Smith’s recognizable patterns of human malformation
|
Temple, I. K.
|
|
2007
|
121 |
5 |
p. 641-642
|
artikel
|
| 22 |
Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region
|
Froyen, Guy
|
|
2007
|
121 |
5 |
p. 539-547
|
artikel
|
| 23 |
Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region
|
Froyen, Guy
|
|
|
121 |
5 |
p. 539-547
|
artikel
|
| 24 |
Molecular diagnostics of Meckel–Gruber syndrome highlights phenotypic differences between MKS1 and MKS3
|
Consugar, Mark B.
|
|
2007
|
121 |
5 |
p. 591-599
|
artikel
|
| 25 |
Molecular diagnostics of Meckel–Gruber syndrome highlights phenotypic differences between MKS1 and MKS3
|
Consugar, Mark B.
|
|
|
121 |
5 |
p. 591-599
|
artikel
|
| 26 |
Novel human pathological mutations
|
|
|
2007
|
121 |
5 |
p. 645-652
|
artikel
|
| 27 |
PGC-1α Thr394Thr and Gly482Ser variants are significantly associated with T2DM in two North Indian populations: a replicate case-control study
|
Bhat, Audesh
|
|
|
121 |
5 |
p. 609-614
|
artikel
|
| 28 |
PGC-1α Thr394Thr and Gly482Ser variants are significantly associated with T2DM in two North Indian populations: a replicate case-control study
|
Bhat, Audesh
|
|
2007
|
121 |
5 |
p. 609-614
|
artikel
|
| 29 |
Testing for association based on excess allele sharing in a sample of related cases and controls
|
Klei, Lambertus
|
|
2007
|
121 |
5 |
p. 549-557
|
artikel
|
| 30 |
Testing for association based on excess allele sharing in a sample of related cases and controls
|
Klei, Lambertus
|
|
|
121 |
5 |
p. 549-557
|
artikel
|
| 31 |
The P239S palladin variant does not account for a significant fraction of hereditary or early onset pancreas cancer
|
Zogopoulous, George
|
|
2007
|
121 |
5 |
p. 635-637
|
artikel
|
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