| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Christopher Baum: Genetic modification of haematopoietic stem cells: methods and protocols
|
Qasim, Waseem
|
|
2010
|
128 |
1 |
p. 119
|
artikel
|
| 2 |
Copy number variants at Williams–Beuren syndrome 7q11.23 region
|
Merla, Giuseppe
|
|
2010
|
128 |
1 |
p. 3-26
|
artikel
|
| 3 |
Dena S. Davis: Genetic Dilemmas: Reproductive Technology, Parental Choices, and Children’s Futures 2/e
|
Douglas, Andrew
|
|
2010
|
128 |
1 |
p. 121-122
|
artikel
|
| 4 |
Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand
|
Phasukkijwatana, Nopasak
|
|
2010
|
128 |
1 |
p. 39-49
|
artikel
|
| 5 |
High-density SNP genotyping detects homogeneity of Spanish and French Basques, and confirms their genomic distinctiveness from other European populations
|
Rodríguez-Ezpeleta, Naiara
|
|
2010
|
128 |
1 |
p. 113-117
|
artikel
|
| 6 |
Obituary of Leena Peltonen-Palotie
|
Hudson, Thomas J.
|
|
2010
|
128 |
1 |
p. 1-2
|
artikel
|
| 7 |
Obituary of Leena Peltonen-Palotie
|
Hudson, Thomas J.
|
|
|
128 |
1 |
p. 1-2
|
artikel
|
| 8 |
The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2)
|
Syx, Delfien
|
|
2010
|
128 |
1 |
p. 79-88
|
artikel
|
| 9 |
The utility and predictive value of combinations of low penetrance genes for screening and risk prediction of colorectal cancer
|
Hawken, Steven J.
|
|
2010
|
128 |
1 |
p. 89-101
|
artikel
|
| 10 |
Transcriptome profile in Williams–Beuren syndrome lymphoblast cells reveals gene pathways implicated in glucose intolerance and visuospatial construction deficits
|
Antonell, Anna
|
|
2010
|
128 |
1 |
p. 27-37
|
artikel
|
| 11 |
Update on molecular diagnosis of hereditary hemorrhagic telangiectasia
|
Richards-Yutz, Jennifer
|
|
2010
|
128 |
1 |
p. 61-77
|
artikel
|
| 12 |
Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophy
|
Iseri, Sibel Ugur
|
|
2010
|
128 |
1 |
p. 51-60
|
artikel
|
| 13 |
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations
|
Friedrich, Katrin
|
|
2010
|
128 |
1 |
p. 103-111
|
artikel
|
Tijdschrift beschrijving