| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A mutation in apolipoprotein A-I in the Iowa type of familial amyloidotic polyneuropathy
|
Nichols, William C.
|
|
1990
|
8 |
2 |
p. 318-323
6 p.
|
artikel
|
| 2 |
Assignment of the human thyroid stimulating hormone receptor (TSHR) gene to chromosome 14q31
|
Rousseau-Merck, M.F.
|
|
1990
|
8 |
2 |
p. 233-236
4 p.
|
artikel
|
| 3 |
Assignment of the porcine calcium release channel gene, a candidate for the malignant hyperthermia locus, to the 6p11 → q21 segment of chromosome 6
|
Harbitz, Ingrid
|
|
1990
|
8 |
2 |
p. 243-248
6 p.
|
artikel
|
| 4 |
Assignment of X-linked hydrocephalus to Xq28 by linkage analysis
|
Willems, Patrick J.
|
|
1990
|
8 |
2 |
p. 367-370
4 p.
|
artikel
|
| 5 |
A testis-specific form of the human pyruvate dehydrogenase E1α subunit is coded for by an intronless gene on chromosome 4
|
Dahl, H.-H.M.
|
|
1990
|
8 |
2 |
p. 225-232
8 p.
|
artikel
|
| 6 |
Batten disease (Spielmeyer-Vogt disease, juvenile onset neuronal ceroid-lipofuscinosis) gene (CLN3) maps to human chromosome 16
|
Gardiner, Mark
|
|
1990
|
8 |
2 |
p. 387-390
4 p.
|
artikel
|
| 7 |
Chromosomal distribution of three members of the human natriuretic peptide receptor/guanylyl cyclase gene family
|
Lowe, David G.
|
|
1990
|
8 |
2 |
p. 304-312
9 p.
|
artikel
|
| 8 |
Chromosomal localization of the genes encoding two forms of the G protein β polypeptide, β1 and β3, in man
|
Levine, Michael A.
|
|
1990
|
8 |
2 |
p. 380-386
7 p.
|
artikel
|
| 9 |
Deletion mapping of the medulloblastoma locus on chromosome 17p
|
Cogen, Philip H.
|
|
1990
|
8 |
2 |
p. 279-285
7 p.
|
artikel
|
| 10 |
DNA sequence polymorphisms in Alu repeats
|
Orita, Masato
|
|
1990
|
8 |
2 |
p. 271-278
8 p.
|
artikel
|
| 11 |
Genetic and physical mapping and population studies of a fibronectin receptor β-subunit-like sequence on human chromosome 19
|
Giuffra, Luis A.
|
|
1990
|
8 |
2 |
p. 340-346
7 p.
|
artikel
|
| 12 |
Genetic heterogeneity in tuberous sclerosis
|
Janssen, L.A.J.
|
|
1990
|
8 |
2 |
p. 237-242
6 p.
|
artikel
|
| 13 |
Genomic analysis of a mouse zinc finger gene, Zfp-35, that is up-regulated during spermatogenesis
|
Cunliffe, Vincent
|
|
1990
|
8 |
2 |
p. 331-339
9 p.
|
artikel
|
| 14 |
Giant G+C% mosaic structures of the human genome found by arrangement of GenBank human DNA sequences according to genetic positions
|
Ikemura, Toshimichi
|
|
1990
|
8 |
2 |
p. 207-216
10 p.
|
artikel
|
| 15 |
Human U1-70K ribonucleoprotein antigen gene: Organization, nucleotide sequence, and mapping to locus 19q13.3
|
Spritz, Richard A.
|
|
1990
|
8 |
2 |
p. 371-379
9 p.
|
artikel
|
| 16 |
Infantile neuronal ceroid-lipofuscinosis is not an allelic form of batten disease: Exclusion of chromosome 16 region with linkage analyses
|
Jokiaho, Irma
|
|
1990
|
8 |
2 |
p. 391-393
3 p.
|
artikel
|
| 17 |
Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families
|
Thakker, R.V.
|
|
1990
|
8 |
2 |
p. 189-193
5 p.
|
artikel
|
| 18 |
Linkage mapping of the highly informative DNA marker D21S156 to human chromosome 21 using a polymorphic GT dinucleotide repeat
|
Lewis, John G.
|
|
1990
|
8 |
2 |
p. 400-402
3 p.
|
artikel
|
| 19 |
Linkage of the multiple endocrine neoplasia type 2B gene (MEN2B) to chromosome 10 markers linked to MEN2A
|
Norum, Robert A.
|
|
1990
|
8 |
2 |
p. 313-317
5 p.
|
artikel
|
| 20 |
Mapping of the gene for CNBP, a finger protein, to human chromosome 3q13.3–q24
|
Lusis, A.J.
|
|
1990
|
8 |
2 |
p. 411-414
4 p.
|
artikel
|
| 21 |
Megabase scale restriction fragment length polymorphisms in the human major histocompatibility complex
|
Lawrance, Simon K.
|
|
1990
|
8 |
2 |
p. 394-399
6 p.
|
artikel
|
| 22 |
Molecular analysis of the Drosophila nuclear lamin gene
|
Osman, Midhat
|
|
1990
|
8 |
2 |
p. 217-224
8 p.
|
artikel
|
| 23 |
Molecular cytotaxonomy of primates by chromosomal in situ suppression hybridization
|
Wienberg, Johannes
|
|
1990
|
8 |
2 |
p. 347-350
4 p.
|
artikel
|
| 24 |
Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pigmentosa families
|
Musarella, M.A.
|
|
1990
|
8 |
2 |
p. 286-296
11 p.
|
artikel
|
| 25 |
Nucleotide sequence of the gene for human transition protein 1 and its chromosomal localization on chromosome 2
|
Luerssen, Hartmut
|
|
1990
|
8 |
2 |
p. 324-330
7 p.
|
artikel
|
| 26 |
Optimizing restriction fragment fingerprinting methods for ordering large genomic libraries
|
Branscomb, E.
|
|
1990
|
8 |
2 |
p. 351-366
16 p.
|
artikel
|
| 27 |
Partial deletions of a sequence family (“DXS278”) and its physical linkage to steroid sulfatase as detected by pulsed-field gel electrophoresis
|
Schnur, Rhonda E.
|
|
1990
|
8 |
2 |
p. 255-262
8 p.
|
artikel
|
| 28 |
Physical mapping by PFGE localizes the COL3A1 and COL5A2 genes to a 35-kb region on human chromosome 2
|
Cutting, Garry R.
|
|
1990
|
8 |
2 |
p. 407-410
4 p.
|
artikel
|
| 29 |
Second-generation approach to the construction of yeast artificial-chromosome libraries
|
Imai, Takashi
|
|
1990
|
8 |
2 |
p. 297-303
7 p.
|
artikel
|
| 30 |
The bovine genome contains polymorphic microsatellites
|
Fries, R.
|
|
1990
|
8 |
2 |
p. 403-406
4 p.
|
artikel
|
| 31 |
The complete sequence of the human β-myosin heavy chain gene and a comparative analysis of its product
|
Jaenicke, Thomas
|
|
1990
|
8 |
2 |
p. 194-206
13 p.
|
artikel
|
| 32 |
Two distinct mutations at the same site in the PCCB gene in propionic acidemia
|
Lamhonwah, Anne-Marie
|
|
1990
|
8 |
2 |
p. 249-254
6 p.
|
artikel
|
| 33 |
Two families of low-copy-number repeats are interspersed on Xp22.3: Implications for the high frequency of deletions in this region
|
Ballabio, Andrea
|
|
1990
|
8 |
2 |
p. 263-270
8 p.
|
artikel
|
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