| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A deletion of two nucleotides in exon 10 of the CFTR gene in a Soviet family with cystic fibrosis causing early infant death
|
Ivaschenko, Tatyana E.
|
|
1991
|
10 |
1 |
p. 298-299
2 p.
|
artikel
|
| 2 |
A genetic linkage map of human chromosome 5 with 60 RFLP loci
|
Weiffenbach, Barbara
|
|
1991
|
10 |
1 |
p. 173-185
13 p.
|
artikel
|
| 3 |
A hybrid cell mapping panel for regional localization of probes to human chromosome 8
|
Wagner, Michael J.
|
|
1991
|
10 |
1 |
p. 114-125
12 p.
|
artikel
|
| 4 |
A linkage map of mouse chromosome 8: Further definition of homologous linkage relationships between mouse chromosome 8 and human chromosomes 8, 16, and 19
|
Howard, Thad A.
|
|
1991
|
10 |
1 |
p. 207-213
7 p.
|
artikel
|
| 5 |
A new system for high-resolution DNA sequence mapping in interphase pronuclei
|
Brandriff, Brigitte
|
|
1991
|
10 |
1 |
p. 75-82
8 p.
|
artikel
|
| 6 |
Assignment of the human pancreatic colipase gene to chromosome 6p21.1 to pter
|
Davis, Richard C.
|
|
1991
|
10 |
1 |
p. 262-265
4 p.
|
artikel
|
| 7 |
cDNA cloning and chromosomal assignment of the endothelin 2 gene: Vasoactive intestinal contractor peptide is rat endothelin 2
|
Bloch, Kenneth D.
|
|
1991
|
10 |
1 |
p. 236-242
7 p.
|
artikel
|
| 8 |
Characterization and chromosomal mapping of a genomic clone encoding human alanine:Glyoxylate aminotransferase
|
Purdue, P.Edward
|
|
1991
|
10 |
1 |
p. 34-42
9 p.
|
artikel
|
| 9 |
Characterization of the human argininosuccinate lyase gene and analysis of exon skipping
|
Abramson, Richard D.
|
|
1991
|
10 |
1 |
p. 126-132
7 p.
|
artikel
|
| 10 |
Chromosomal mapping of glutamate dehydrogenase gene sequences to mouse chromosomes 7 and 14
|
Tzimagiorgis, George
|
|
1991
|
10 |
1 |
p. 83-88
6 p.
|
artikel
|
| 11 |
Complete structure of the human gene encoding neuron-specific enolase
|
Oliva, Daniele
|
|
1991
|
10 |
1 |
p. 157-165
9 p.
|
artikel
|
| 12 |
Deletion mapping of DNA segments from the Y chromosome long arm and their analysis in an XX male
|
Donlon, Timothy A.
|
|
1991
|
10 |
1 |
p. 51-56
6 p.
|
artikel
|
| 13 |
Detection of three rare frameshift mutations in the cystic fibrosis gene in an African-American (CF444delA), an Italian (CF2522insC), and a Soviet (CF3821delT)1
|
White, Marga Belle
|
|
1991
|
10 |
1 |
p. 266-269
4 p.
|
artikel
|
| 14 |
Erratum
|
|
|
1991
|
10 |
1 |
p. 300-
1 p.
|
artikel
|
| 15 |
EVX2, a human homeobox gene homologous to the even-skipped segmentation gene, is localized at the 5′ end of HOX4 locus on chromosome 2
|
D'Esposito, Maurizio
|
|
1991
|
10 |
1 |
p. 43-50
8 p.
|
artikel
|
| 16 |
Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene
|
Zielenski, Julian
|
|
1991
|
10 |
1 |
p. 214-228
15 p.
|
artikel
|
| 17 |
G protein Gsα (GNAS1), the probable candidate gene for albright hereditary osteodystrophy, is assigned to human chromosome 20q12–q13.2
|
Gopal Rao, V.V.N.
|
|
1991
|
10 |
1 |
p. 257-261
5 p.
|
artikel
|
| 18 |
High-density molecular map of the central span of the mouse X chromosome
|
Brockdorff, N.
|
|
1991
|
10 |
1 |
p. 17-22
6 p.
|
artikel
|
| 19 |
Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene
|
Zielenski, Julian
|
|
1991
|
10 |
1 |
p. 229-235
7 p.
|
artikel
|
| 20 |
Isolation and regional mapping of NotI and EagI clones from human chromosome 21
|
Gao, Jizong
|
|
1991
|
10 |
1 |
p. 166-172
7 p.
|
artikel
|
| 21 |
Isolation, characterization, and chromosomal mapping of mouse P450 17α-hydroxylase/C17–20 lyase
|
Youngblood, Geri L.
|
|
1991
|
10 |
1 |
p. 270-275
6 p.
|
artikel
|
| 22 |
Isolation of a variant family of mouse minor satellite DNA that hybridizes preferentially to chromosome 4
|
Broccoli, Dominique
|
|
1991
|
10 |
1 |
p. 68-74
7 p.
|
artikel
|
| 23 |
Linear order of new and established DNA markers around the fragile site at Xq27.3
|
Hirst, M.C.
|
|
1991
|
10 |
1 |
p. 243-249
7 p.
|
artikel
|
| 24 |
Linkage of amelogenin (Amel) to the distal portion of the mouse X chromosome
|
Chapman, Verne M.
|
|
1991
|
10 |
1 |
p. 23-28
6 p.
|
artikel
|
| 25 |
Localization of CYP2F1 by multipoint linkage analysis and pulsed-field gel electrophoresis
|
Bale, Allen E.
|
|
1991
|
10 |
1 |
p. 284-286
3 p.
|
artikel
|
| 26 |
Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22–Xp11.3
|
Kwan, Sau-Ping
|
|
1991
|
10 |
1 |
p. 29-33
5 p.
|
artikel
|
| 27 |
Mapping nonisotopically labeled DNA probes to human chromosome bands by confocal microscopy
|
Albertson, Donna G.
|
|
1991
|
10 |
1 |
p. 143-150
8 p.
|
artikel
|
| 28 |
Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome
|
Scambler, Peter J.
|
|
1991
|
10 |
1 |
p. 201-206
6 p.
|
artikel
|
| 29 |
Molecular characterization of a deletion encompassing the splotch mutation on mouse chromosome 1
|
Epstein, Douglas J.
|
|
1991
|
10 |
1 |
p. 89-93
5 p.
|
artikel
|
| 30 |
Molecular characterization of rat multigene family encoding proline-rich proteins
|
Lin, Her H.
|
|
1991
|
10 |
1 |
p. 102-113
12 p.
|
artikel
|
| 31 |
Nonhomologous recombination in the human genome: Deletions in the human factor VIII gene
|
Woods-Samuels, Patricia
|
|
1991
|
10 |
1 |
p. 94-101
8 p.
|
artikel
|
| 32 |
Ornithine aminotransferase-related sequences map to two nonadjacent intervals on the human X chromosome short arm
|
Lafreniere, Ronald G.
|
|
1991
|
10 |
1 |
p. 276-279
4 p.
|
artikel
|
| 33 |
Parental origin of chromosome 22 loss in sporadic and NF2 neuromas
|
Fontaine, Bertrand
|
|
1991
|
10 |
1 |
p. 280-283
4 p.
|
artikel
|
| 34 |
Polyamines eliminate an extreme size bias against transformation of large yeast artificial chromosome DNA
|
Connelly, Carla
|
|
1991
|
10 |
1 |
p. 10-16
7 p.
|
artikel
|
| 35 |
Sequences of junction fragments in the deletion-prone region of the dystrophin gene
|
Love, D.R.
|
|
1991
|
10 |
1 |
p. 57-67
11 p.
|
artikel
|
| 36 |
Smallest region of overlap in Wilms tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus
|
Ton, Carl C.T.
|
|
1991
|
10 |
1 |
p. 293-297
5 p.
|
artikel
|
| 37 |
Structural organization and complete sequence of the human α-N-acetylgalactosaminidase gene: Homology with the α-galactosidase A gene provides evidence for evolution from a common ancestral gene
|
Wang, Anne M.
|
|
1991
|
10 |
1 |
p. 133-142
10 p.
|
artikel
|
| 38 |
Structure of the human cytochrome c oxidase subunit Vb gene and chromosomal mapping of the coding gene and of seven pseudogenes
|
Lomax, Margaret I.
|
|
1991
|
10 |
1 |
p. 1-9
9 p.
|
artikel
|
| 39 |
Structure of the murine c-sis proto-oncogene (Sis, PDGFB) encoding the B chain of platelet-derived growth factor
|
Bonthron, David T.
|
|
1991
|
10 |
1 |
p. 287-292
6 p.
|
artikel
|
| 40 |
The gene for SP-40,40, human homolog of rat sulfated glycoprotein 2, rat clusterin, and rat testosterone-repressed prostate message 2, maps to chromosome 8
|
Purrello, Michele
|
|
1991
|
10 |
1 |
p. 151-156
6 p.
|
artikel
|
| 41 |
The human chromosome content in human × rodent somatic cell hybrids analyzed by a screening technique using Alu PCR
|
Bicknell, David C.
|
|
1991
|
10 |
1 |
p. 186-192
7 p.
|
artikel
|
| 42 |
The human connexin gene family of gap junction proteins: Distinct chromosomal locations but similar structures
|
Fishman, Glenn I.
|
|
1991
|
10 |
1 |
p. 250-256
7 p.
|
artikel
|
| 43 |
The search for South European cystic fibrosis mutations: Identification of two new mutations, four variants, and intronic sequences
|
Gasparini, P.
|
|
1991
|
10 |
1 |
p. 193-200
8 p.
|
artikel
|
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