| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Additional polymorphism at a CHR 9 reference locus (D9S12)
|
Yuille, M.A.R.
|
|
1992
|
1 |
5 |
p. 351-351
|
article
|
| 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
|
article
|
| 3 |
A Rsal polymorphism in the ERCC2 locus
|
von Deimling, A.
|
|
1992
|
1 |
5 |
p. 355-355
|
article
|
| 4 |
A two-allele Pstl RFLP for the alpha-1C adrenergic receptor gene (ADRA1C)
|
Hoehe, Margret R.
|
|
1992
|
1 |
5 |
p. 349-349
|
article
|
| 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
|
article
|
| 6 |
Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome
|
Baird, Paul N.
|
|
1992
|
1 |
5 |
p. 301-305
|
article
|
| 7 |
Dinucleotide repeat polymorphism at the D21S65 locus
|
Goto, J.
|
|
1992
|
1 |
5 |
p. 350-350
|
article
|
| 8 |
Dinucleotide repeat polymorphism at the D4S251 locus
|
Petrukhin, Konstantin E.
|
|
1992
|
1 |
5 |
p. 349-349
|
article
|
| 9 |
Dinucleotide repeat polymorphism at the GABAA receptor α5 (GABRA5) locus at chromosome 15q11-q13
|
Glatt, Karen A.
|
|
1992
|
1 |
5 |
p. 348-348
|
article
|
| 10 |
Dinucleotide repeat polymorphism at the human gene for the brainderived neurotrophic factor (BDNF)
|
Pröschel, Michael
|
|
1992
|
1 |
5 |
p. 353-353
|
article
|
| 11 |
Dinucleotide repeat polymorphism in the human estrogen receptor (ESR) gene
|
Senno, L.del
|
|
1992
|
1 |
5 |
p. 354-354
|
article
|
| 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
|
article
|
| 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
|
article
|
| 14 |
Improving the polymorphism content of the 3′ UTR of the human IGF2R gene
|
Hol, F.A.
|
|
1992
|
1 |
5 |
p. 347-347
|
article
|
| 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
|
article
|
| 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
|
article
|
| 17 |
SAM 1.1 and JOSH 4.4: two RFLPs within the human DCC gene
|
Simons, J.W.
|
|
1992
|
1 |
5 |
p. 352-352
|
article
|
| 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
|
article
|
| 19 |
Taql polymorphism at the alanine: glyoxylate aminotransferase (AGXT) gene locus
|
Rumsby, G.
|
|
1992
|
1 |
5 |
p. 350-350
|
article
|
| 20 |
The ‘colorizing’ of cytogenetics: is it ready for prime time?
|
Ledbetter, David H.
|
|
1992
|
1 |
5 |
p. 297-299
|
article
|
| 21 |
Two Mspl polymorphisms within the APC gene
|
Cottrell, S.
|
|
1992
|
1 |
5 |
p. 352-352
|
article
|
| 22 |
Two Taql polymorphisms at the human PGM1 locus
|
Hollyoake, M.
|
|
1992
|
1 |
5 |
p. 354-354
|
article
|
Journal description