| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Alphoid DNA polymorphisms for chromosome 21 can be distinguished from those of chromosome 13 using probes homologous to both
|
Jabs, Ethylin Wang
|
|
1991
|
9 |
1 |
p. 141-146
6 p.
|
artikel
|
| 2 |
A map of the distal region of the long arm of human chromosome 21 constructed by radiation hybrid mapping and pulsed-field gel electrophoresis
|
Burmeister, Margit
|
|
1991
|
9 |
1 |
p. 19-30
12 p.
|
artikel
|
| 3 |
An approach to the use of stable isotopes for DNA sequencing
|
Jacobson, K.Bruce
|
|
1991
|
9 |
1 |
p. 51-59
9 p.
|
artikel
|
| 4 |
An unusually proximal deletion on the short arm of chromosome 3 in a patient with small cell lung cancer
|
Daly, M.C.
|
|
1991
|
9 |
1 |
p. 113-119
7 p.
|
artikel
|
| 5 |
A simple method for ordering loci using data from radiation hybrids
|
Falk, C.T.
|
|
1991
|
9 |
1 |
p. 120-123
4 p.
|
artikel
|
| 6 |
A yeast artificial chromosome contig encompassing the cystic fibrosis locus
|
Anand, R.
|
|
1991
|
9 |
1 |
p. 124-130
7 p.
|
artikel
|
| 7 |
Characterization of the 3′ half of the human type IV collagen α5 gene that is affected in the Alport syndrome
|
Zhou, Jing
|
|
1991
|
9 |
1 |
p. 1-9
9 p.
|
artikel
|
| 8 |
Chromosomal localization of two human zinc finger protein genes, ZNF24 (KOX17) and ZNF29 (KOX26), to 18q12 and 17p13–p12, respectively
|
Rousseau-Merck, M.F.
|
|
1991
|
9 |
1 |
p. 154-161
8 p.
|
artikel
|
| 9 |
Chromosomal location of murine and human IL-1 receptor genes
|
Copeland, Neal G.
|
|
1991
|
9 |
1 |
p. 44-50
7 p.
|
artikel
|
| 10 |
Chromosome 22 Workshop Proceedings
|
Kaplan, Jean-Claude
|
|
1991
|
9 |
1 |
p. 214-218
5 p.
|
artikel
|
| 11 |
Development of human chromosome-specific PCR primers for characterization of somatic cell hybrids
|
Abbott, Cathy
|
|
1991
|
9 |
1 |
p. 73-77
5 p.
|
artikel
|
| 12 |
Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A
|
Lairmore, Terry C.
|
|
1991
|
9 |
1 |
p. 181-192
12 p.
|
artikel
|
| 13 |
Genetic mapping of new RFLPs at Xq27–q28
|
Suthers, G.K.
|
|
1991
|
9 |
1 |
p. 37-43
7 p.
|
artikel
|
| 14 |
Genetic mapping of the lurcher locus on mouse chromosome 6 using an intersubspecific backcross
|
Norman, Deborah J.
|
|
1991
|
9 |
1 |
p. 147-153
7 p.
|
artikel
|
| 15 |
Genetic maps of mouse Chromosome 17 including 12 new anonymous DNA loci and 25 anchor loci
|
Nadeau, Joseph H.
|
|
1991
|
9 |
1 |
p. 78-89
12 p.
|
artikel
|
| 16 |
Human thymosin- β4 6–26 gene is part of a multigene family composed of seven members located on seven different chromosomes
|
Clauss, Isabelle M.
|
|
1991
|
9 |
1 |
p. 174-180
7 p.
|
artikel
|
| 17 |
Identification of CpG islands in a physical map encompassing the Friedreich's ataxia locus
|
Wilkes, David
|
|
1991
|
9 |
1 |
p. 90-95
6 p.
|
artikel
|
| 18 |
Increased recombination adjacent to the Huntington disease-linked D4S10 marker
|
Allitto, Bernice A.
|
|
1991
|
9 |
1 |
p. 104-112
9 p.
|
artikel
|
| 19 |
Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1
|
Järvelä, Irma
|
|
1991
|
9 |
1 |
p. 170-173
4 p.
|
artikel
|
| 20 |
Isolation of region-specific and polymorphic markers from chromosome 17 by restricted Alu polymerase chain reaction
|
Guzzetta, Vito
|
|
1991
|
9 |
1 |
p. 31-36
6 p.
|
artikel
|
| 21 |
Localization of a 900-bp-long fragment of the human choline acetyltransferase gene to 10q11.2 by nonradioactive in situ hybridization
|
Viegas-Péquignot, Evani
|
|
1991
|
9 |
1 |
p. 210-212
3 p.
|
artikel
|
| 22 |
Localization of monocyte chemotactic protein-1 gene (SCYA2) to human chromosome 17q11.2–q21.1
|
Mehrabian, Margarete
|
|
1991
|
9 |
1 |
p. 200-203
4 p.
|
artikel
|
| 23 |
Mapping of the gene for human cysteine proteinase inhibitor stefin A, STF1, to chromosome 3cen-q21
|
Hsieh, Wang-Ting
|
|
1991
|
9 |
1 |
p. 207-209
3 p.
|
artikel
|
| 24 |
Molecular mapping of albino deletions associated with early embryonic lethality in the mouse
|
Niswander, Lee
|
|
1991
|
9 |
1 |
p. 162-169
8 p.
|
artikel
|
| 25 |
Mouse ferritin H sequences map to chromosomes 3, 6, and 19
|
Yachou, A.
|
|
1991
|
9 |
1 |
p. 204-206
3 p.
|
artikel
|
| 26 |
Phenylalanine hydroxylase gene: Novel missense mutation in exon 7 causing severe phenylketonuria
|
Dworniczak, Bernd
|
|
1991
|
9 |
1 |
p. 193-199
7 p.
|
artikel
|
| 27 |
Phenylketonuria missense mutations in the Mediterranean
|
Okano, Yoshiyuki
|
|
1991
|
9 |
1 |
p. 96-103
8 p.
|
artikel
|
| 28 |
Single base mutation in α5(IV) collagen chain gene converting a conserved cysteine to serine in Alport syndrome
|
Zhou, Jing
|
|
1991
|
9 |
1 |
p. 10-18
9 p.
|
artikel
|
| 29 |
Structure of the gorilla α-fetoprotein gene and the divergence of primates
|
Ryan, Susan C.
|
|
1991
|
9 |
1 |
p. 60-72
13 p.
|
artikel
|
| 30 |
The exon-intron organization of the human erythrocyte α-spectrin gene
|
Kotula, Leszek
|
|
1991
|
9 |
1 |
p. 131-140
10 p.
|
artikel
|
| 31 |
Workshop on Human Chromosome 3
|
Naylor, Susan L.
|
|
1991
|
9 |
1 |
p. 213-214
2 p.
|
artikel
|
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