nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Additional polymorphism at a CHR 9 reference locus (D9S12)
|
Yuille, M.A.R. |
|
1992 |
1 |
5 |
p. 351-351 |
artikel |
2 |
An Mspl RFLP in the human ARNT gene, encoding a subunit of the nuclear form of the Ah (dioxin) receptor
|
Johnson, Barton S. |
|
1992 |
1 |
5 |
p. 351-351 |
artikel |
3 |
A Rsal polymorphism in the ERCC2 locus
|
von Deimling, A. |
|
1992 |
1 |
5 |
p. 355-355 |
artikel |
4 |
A two-allele Pstl RFLP for the alpha-1C adrenergic receptor gene (ADRA1C)
|
Hoehe, Margret R. |
|
1992 |
1 |
5 |
p. 349-349 |
artikel |
5 |
Cloning and characterization of the inversion breakpoint at chromosome 2q35 in a patient with Waardenburg syndrome type I
|
Tsukamoto, Kazuhiro |
|
1992 |
1 |
5 |
p. 315-317 |
artikel |
6 |
Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome
|
Baird, Paul N. |
|
1992 |
1 |
5 |
p. 301-305 |
artikel |
7 |
Dinucleotide repeat polymorphism at the D21S65 locus
|
Goto, J. |
|
1992 |
1 |
5 |
p. 350-350 |
artikel |
8 |
Dinucleotide repeat polymorphism at the D4S251 locus
|
Petrukhin, Konstantin E. |
|
1992 |
1 |
5 |
p. 349-349 |
artikel |
9 |
Dinucleotide repeat polymorphism at the GABAA receptor α5 (GABRA5) locus at chromosome 15q11-q13
|
Glatt, Karen A. |
|
1992 |
1 |
5 |
p. 348-348 |
artikel |
10 |
Dinucleotide repeat polymorphism at the human gene for the brainderived neurotrophic factor (BDNF)
|
Pröschel, Michael |
|
1992 |
1 |
5 |
p. 353-353 |
artikel |
11 |
Dinucleotide repeat polymorphism in the human estrogen receptor (ESR) gene
|
Senno, L.del |
|
1992 |
1 |
5 |
p. 354-354 |
artikel |
12 |
Dominant negative mutations in the Wilms tumour (WT1) gene cause Denys-Drash syndrome—proof that a tumour-suppressor gene plays a crucial role in normal genitourinary development
|
Hastie, Nicholas D. |
|
1992 |
1 |
5 |
p. 293-295 |
artikel |
13 |
D20S19, linked to low voltage EEG, benign neonatal convulsions, and Fanconi anaemia, maps to a region of enhanced recombination and is localized between CpG islands
|
Steinlein, Ortrud |
|
1992 |
1 |
5 |
p. 325-329 |
artikel |
14 |
Improving the polymorphism content of the 3′ UTR of the human IGF2R gene
|
Hol, F.A. |
|
1992 |
1 |
5 |
p. 347-347 |
artikel |
15 |
Isolation and mapping to 17p12 – 13 of the human homologous of the murine growth arrest specific Gas-3 gene
|
Martinotti, Alessia |
|
1992 |
1 |
5 |
p. 331-334 |
artikel |
16 |
Multicolor fluorescence in situ hybridization for the simultaneous detection of probe sets for chromosomes 13, 18, 21, X and Y in uncultured amniotic fluid cells
|
Ried, Thomas |
|
1992 |
1 |
5 |
p. 307-313 |
artikel |
17 |
SAM 1.1 and JOSH 4.4: two RFLPs within the human DCC gene
|
Simons, J.W. |
|
1992 |
1 |
5 |
p. 352-352 |
artikel |
18 |
Single base polymorphism in the human Tumour Necrosis Factor alpha (TNFα) gene detectable by Ncol restriction of PCR product
|
Wilson, A.G. |
|
1992 |
1 |
5 |
p. 353-353 |
artikel |
19 |
Taql polymorphism at the alanine: glyoxylate aminotransferase (AGXT) gene locus
|
Rumsby, G. |
|
1992 |
1 |
5 |
p. 350-350 |
artikel |
20 |
The ‘colorizing’ of cytogenetics: is it ready for prime time?
|
Ledbetter, David H. |
|
1992 |
1 |
5 |
p. 297-299 |
artikel |
21 |
Two Mspl polymorphisms within the APC gene
|
Cottrell, S. |
|
1992 |
1 |
5 |
p. 352-352 |
artikel |
22 |
Two Taql polymorphisms at the human PGM1 locus
|
Hollyoake, M. |
|
1992 |
1 |
5 |
p. 354-354 |
artikel |