| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Alu polymorphism in the human type I Keratin (KRT14) gene
|
Humphries, M.M.
|
|
1992
|
1 |
6 |
p. 453-453
|
artikel
|
| 2 |
A microsatellite polymorphic probe on chromosome 3p: λLIB12–2CATT (D3S1244)
|
Li, Hua
|
|
1992
|
1 |
6 |
p. 452-452
|
artikel
|
| 3 |
A molecular deletion map of the Y chromosome long arm defining X and autosomal homologous regions and the localisation of the HYA locus to the proximal region of the Yq euchromatin
|
O'Reilly, Amanda J.
|
|
1992
|
1 |
6 |
p. 379-385
|
artikel
|
| 4 |
Author index
|
|
|
1992
|
1 |
6 |
p. 457-457
|
artikel
|
| 5 |
(CA)n-dinucleotide repeat polymorphism at the locus for the alpha2C adrenergic receptor (ADRA2C) on 4p16
|
Riess, Olaf
|
|
1992
|
1 |
6 |
p. 452-452
|
artikel
|
| 6 |
Characterization of mutations in phenotypic variants of hypoxanthine phosphoribosyltransferase deficiency
|
Sege-Peterson, Karin
|
|
1992
|
1 |
6 |
p. 427-432
|
artikel
|
| 7 |
Characterization of the human HOX 7 cDNA and identification of polymorphic markers
|
Padanilam, B.J.
|
|
1992
|
1 |
6 |
p. 407-410
|
artikel
|
| 8 |
Deletion in the prion protein gene in a demented patient
|
Diedrich, J.F.
|
|
1992
|
1 |
6 |
p. 443-444
|
artikel
|
| 9 |
Dinucleotide repeat polymorphism at the D1S182 locus
|
Petrukhin, Konstantin E.
|
|
1992
|
1 |
6 |
p. 454-454
|
artikel
|
| 10 |
Dinucleotide repeat polymorphism at the D5S253 locus
|
Bernard, L.E.
|
|
1992
|
1 |
6 |
p. 455-455
|
artikel
|
| 11 |
Dinucleotide repeat polymorphism at the D19S206 locus
|
Petrukhin, Konstantin E.
|
|
1992
|
1 |
6 |
p. 454-454
|
artikel
|
| 12 |
Dinucleotide repeat polymorphism at the RBP3 locus in chromosome band 10q11.2
|
Papi, L.
|
|
1992
|
1 |
6 |
p. 450-450
|
artikel
|
| 13 |
Dinucleotide repeat polymorphism at the topoisomerase (DNA) I pseudogene 2 (TOPIP2)
|
Trofatter, J.A.
|
|
1992
|
1 |
6 |
p. 455-455
|
artikel
|
| 14 |
EcoRV RFLP of the desmin (DES) gene and Mspl RFLP of the villin (VIL1) gene on human chromosome 2
|
Shaw, M.A.
|
|
1992
|
1 |
6 |
p. 448-448
|
artikel
|
| 15 |
Four dinucleotide repeat polymorphisms on chromosome 9 (D9S143–146)
|
Furlong, Robert A.
|
|
1992
|
1 |
6 |
p. 447-447
|
artikel
|
| 16 |
Human CC10, the homologue of rabbit uteroglobin: genomic cloning, chromosomal localization and expression in endometrial cell lines
|
Wolf, Markus
|
|
1992
|
1 |
6 |
p. 371-378
|
artikel
|
| 17 |
Identification of genes using oligonucleotides corresponding to splice site consensus sequences
|
Melmer, Georg
|
|
1992
|
1 |
6 |
p. 433-438
|
artikel
|
| 18 |
Insertion/deletion polymorphism at D19S95 associated with the myotonic dystrophy CTG repeat
|
Crow, S.R.
|
|
1992
|
1 |
6 |
p. 451-451
|
artikel
|
| 19 |
Long-term persistence of plasmid DNA and foreign gone expression in mouse muscle
|
Wolff, Jon A.
|
|
1992
|
1 |
6 |
p. 363-369
|
artikel
|
| 20 |
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11–13) by YAC cloning and FISH analysis
|
Kuwano, Akira
|
|
1992
|
1 |
6 |
p. 417-425
|
artikel
|
| 21 |
Rapid and simultaneous detection of multiple mutations by pooled and multiplex single nucleotide primer extension: application to the study of insulin-responsive glucose transporter and insulin receptor mutations in non-insulindependent diabetes
|
Krook, Anna
|
|
1992
|
1 |
6 |
p. 391-395
|
artikel
|
| 22 |
Single base polymorphism at −511 in the human interleukin-1β gene (IL1β)
|
Giovine, F.S. di
|
|
1992
|
1 |
6 |
p. 450-450
|
artikel
|
| 23 |
SSCP polymorphism in the human hepatic triglyceride lipase (LIPC) gene
|
Reina, M.
|
|
1992
|
1 |
6 |
p. 453-453
|
artikel
|
| 24 |
Taql and Bsu361 polymorphisms in the human glycoprotein Ibα gene (GPIBα)
|
Petersen, E.J.
|
|
1992
|
1 |
6 |
p. 451-451
|
artikel
|
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