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 |