| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A cluster of expressed zinc finger protein genes in the pericentromeric region of human chromosome 10
|
Rousseau-Merck, M.F.
|
|
1992
|
13 |
3 |
p. 845-848
4 p.
|
artikel
|
| 2 |
A high-resolution meiotic mapping panel for the pericentromeric region of chromosome 10
|
Lichter, Jay B.
|
|
1992
|
13 |
3 |
p. 607-612
6 p.
|
artikel
|
| 3 |
A microsatellite polymorphism associated with the PLC1 (phospholipase C) locus: Identification, mapping, and linkage to the MODY locus on chromosome 20
|
Rothschild, Cynthia B.
|
|
1992
|
13 |
3 |
p. 560-564
5 p.
|
artikel
|
| 4 |
A missense mutation (Asp250→Asn) in exon 6 of the human lipoprotein lipase gene causes chylomicronemia in patients of different ancestries
|
Ma, Yuanhong
|
|
1992
|
13 |
3 |
p. 649-653
5 p.
|
artikel
|
| 5 |
A new mutation (1078delT) in exon 7 of the CFTR gene in a southern French adult with cystic fibrosis
|
Claustres, Mireille
|
|
1992
|
13 |
3 |
p. 907-908
2 p.
|
artikel
|
| 6 |
A preliminary linkage map of the chicken genome
|
Bumstead, Nat
|
|
1992
|
13 |
3 |
p. 690-697
8 p.
|
artikel
|
| 7 |
A radiation hybrid map of 18 growth factor, growth factor receptor, hormone receptor, or neurotransmitter receptor genes on the distal region of the long arm of chromosome 5
|
Warrington, J.A.
|
|
1992
|
13 |
3 |
p. 803-808
6 p.
|
artikel
|
| 8 |
A radiation-reduced hybrid cell line containing 5 Mb/17 cM of human DNA from 9q34
|
Henske, Elizabeth P.
|
|
1992
|
13 |
3 |
p. 841-844
4 p.
|
artikel
|
| 9 |
A single serine:pyruvate aminotransferase gene on rat chromosome 9q34-q36
|
Mori, Masayuki
|
|
1992
|
13 |
3 |
p. 686-689
4 p.
|
artikel
|
| 10 |
Assignment of the human 2′,3′-cyclic nucleotide 3′-phosphohydrolase gene to chromosome 17
|
Sprinkle, T.J.
|
|
1992
|
13 |
3 |
p. 877-880
4 p.
|
artikel
|
| 11 |
Assignment of the human stromelysin 3 (STMY3) gene to the q11.2 region of chromosome 22
|
Levy, Annie
|
|
1992
|
13 |
3 |
p. 881-883
3 p.
|
artikel
|
| 12 |
Assignment of two human cell cycle genes, CDC25C and CCNB1, to 5q31 and 5q12, respectively
|
Sartor, Heino
|
|
1992
|
13 |
3 |
p. 911-912
2 p.
|
artikel
|
| 13 |
A transposon-like element in the deletion-prone region of the dystrophin gene
|
Pizzuti, Antonio
|
|
1992
|
13 |
3 |
p. 594-600
7 p.
|
artikel
|
| 14 |
A yeast artificial chromosome contig encompassing the type 1 neurofibromatosis gene
|
Marchuk, Douglas A.
|
|
1992
|
13 |
3 |
p. 672-680
9 p.
|
artikel
|
| 15 |
cDNA Sequence of human p11 calpactin I light chain
|
Dooley, Thomas P.
|
|
1992
|
13 |
3 |
p. 866-868
3 p.
|
artikel
|
| 16 |
Characterization and chromosomal mapping of the gene encoding the cellular DNA binding protein HTLF
|
Li, Ching
|
|
1992
|
13 |
3 |
p. 658-664
7 p.
|
artikel
|
| 17 |
Characterization and chromosomal mapping of the gene encoding the cellular DNA binding protein ILF
|
Li, Ching
|
|
1992
|
13 |
3 |
p. 665-671
7 p.
|
artikel
|
| 18 |
Characterization of a highly polymorphic region near the first exon of the human MAOA gene containing a GT dinucleotide and a novel VNTR motif
|
Hinds, Heather L.
|
|
1992
|
13 |
3 |
p. 896-897
2 p.
|
artikel
|
| 19 |
Characterization of a YAC and cosmid contig containing markers tightly linked to the myotonic dystrophy locus on chromosome 19
|
Buxton, Jessica
|
|
1992
|
13 |
3 |
p. 526-531
6 p.
|
artikel
|
| 20 |
Characterization of human adenylate kinase 3 (AK3) cDNA and mapping of the AK3 pseudogene to an intron of the NF1 gene
|
Xu, Gangfeng
|
|
1992
|
13 |
3 |
p. 537-542
6 p.
|
artikel
|
| 21 |
Chromosomal localization of an SH2-containing tyrosine phosphatase (PTPN6)
|
Plutzky, J.
|
|
1992
|
13 |
3 |
p. 869-872
4 p.
|
artikel
|
| 22 |
Cloning of six new genes with zinc finger motifs mapping to short and long arms of human acrocentric chromosome 22 (p and q11.2)
|
Aubry, Muriel
|
|
1992
|
13 |
3 |
p. 641-648
8 p.
|
artikel
|
| 23 |
Colocalization of the genes for the α3(IV) and α4(IV) chains of type IV collagen to chromosome 2 bands q35–q37
|
Mariyama, Mariko
|
|
1992
|
13 |
3 |
p. 809-813
5 p.
|
artikel
|
| 24 |
Construction, analysis, and application of a radiation hybrid mapping panel surrounding the mouse agouti locus
|
Ollmann, Michael M.
|
|
1992
|
13 |
3 |
p. 731-740
10 p.
|
artikel
|
| 25 |
Continuous linkage map of human chromosome 14 short tandem repeat polymorphisms
|
Wang, Zhenyuan
|
|
1992
|
13 |
3 |
p. 532-536
5 p.
|
artikel
|
| 26 |
CpG suppression in vertebrate genomes does not account for the rarity of (CpG) n microsatellite repeats
|
Stallings, Raymond L.
|
|
1992
|
13 |
3 |
p. 890-891
2 p.
|
artikel
|
| 27 |
Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer
|
Telenius, Ha˚kan
|
|
1992
|
13 |
3 |
p. 718-725
8 p.
|
artikel
|
| 28 |
Detection of mutations in the factor VIII gene using single-stranded conformational polymorphism (SSCP)
|
Economou, Effrosini P.
|
|
1992
|
13 |
3 |
p. 909-911
3 p.
|
artikel
|
| 29 |
Detection of point mutations and a gross deletion in six Hunter Syndrome patients
|
Flomen, Rachel H.
|
|
1992
|
13 |
3 |
p. 543-550
8 p.
|
artikel
|
| 30 |
Erratum
|
|
|
1992
|
13 |
3 |
p. 915-
1 p.
|
artikel
|
| 31 |
Expressed sequence tags and chromosomal localization of cDNA clones from a subtracted retinal pigment epithelium library
|
Gieser, Linn
|
|
1992
|
13 |
3 |
p. 873-876
4 p.
|
artikel
|
| 32 |
Familial amyloidosis, Finnish type: G654 → A mutation of the gelsolin gene in Finnish families and an unrelated American family
|
de la Chapelle, A.
|
|
1992
|
13 |
3 |
p. 898-901
4 p.
|
artikel
|
| 33 |
Fluorescence in situ hybridization of YAC clones after Alu-PCR amplification
|
Lengauer, Christoph
|
|
1992
|
13 |
3 |
p. 826-828
3 p.
|
artikel
|
| 34 |
Gene-centromere linkage mapping by PCR analysis of individual oocytes
|
Cui, Xiangfeng
|
|
1992
|
13 |
3 |
p. 713-717
5 p.
|
artikel
|
| 35 |
Gene-dosage mapping of 30 DNA markers on chromosome 21
|
Delabar, Jean-Maurice
|
|
1992
|
13 |
3 |
p. 887-889
3 p.
|
artikel
|
| 36 |
Genomic organization, chromosomal localization, and independent expression of human cyclin D genes
|
Inaba, Toshiya
|
|
1992
|
13 |
3 |
p. 565-574
10 p.
|
artikel
|
| 37 |
Genomic organization, sequence analysis, and chromosomal localization of the human car☐yl ester lipase (CEL) gene and a CEL-like (CELL) gene
|
Lidberg, Ulf
|
|
1992
|
13 |
3 |
p. 630-640
11 p.
|
artikel
|
| 38 |
Genomic sequence and chromosomal location of human interleukin-11 gene (IL11)
|
McKinley, Denise
|
|
1992
|
13 |
3 |
p. 814-819
6 p.
|
artikel
|
| 39 |
Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease
|
Maury, C.P.J.
|
|
1992
|
13 |
3 |
p. 902-903
2 p.
|
artikel
|
| 40 |
Identification of a CA repeat at the TCRA locus using yeast artificial chromosomes: A general method for generating highly polymorphic markers at chosen loci
|
Corne´lis, François
|
|
1992
|
13 |
3 |
p. 820-825
6 p.
|
artikel
|
| 41 |
Identification of three novel missense PKU mutations among Chinese
|
Li, Jia
|
|
1992
|
13 |
3 |
p. 894-895
2 p.
|
artikel
|
| 42 |
Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms
|
Hudson, Thomas J.
|
|
1992
|
13 |
3 |
p. 622-629
8 p.
|
artikel
|
| 43 |
Isolation and high-resolution mapping of new DNA markers from the pericentromeric region of chromosome 10
|
Miller, D.L.
|
|
1992
|
13 |
3 |
p. 601-606
6 p.
|
artikel
|
| 44 |
Localization of a bile acid UDP-glucuronosyltransferase gene (UGT2B) to chromosome 4 using the polymerase chain reaction
|
Monaghan, Gemma
|
|
1992
|
13 |
3 |
p. 908-909
2 p.
|
artikel
|
| 45 |
Localization of the gene coding for ventricular myosin regulatory light chain (MYL2) to human chromosome 12q23-q24.3
|
Macera, M.J.
|
|
1992
|
13 |
3 |
p. 829-831
3 p.
|
artikel
|
| 46 |
MAF45, a highly polymorphic marker for the pseudoautosomal region of the sheep genome, is not linked to the fecXI (Inverdale) gene
|
Swarbrick, Peter A.
|
|
1992
|
13 |
3 |
p. 849-851
3 p.
|
artikel
|
| 47 |
Mapping of the motor neuron degeneration (Mnd) gene, a mouse model of amyotrophic lateral sclerosis (ALS)
|
Messer, Anne
|
|
1992
|
13 |
3 |
p. 797-802
6 p.
|
artikel
|
| 48 |
Mapping of two chromosome 15 microsatellites
|
Fougerousse, F.
|
|
1992
|
13 |
3 |
p. 903-904
2 p.
|
artikel
|
| 49 |
Mapping the human liver/islet glucose transporter (GLUT2) gene within a genetic linkage map of chromosome 3q using a (CA) n dinucleotide repeat polymorphism and characterization of the polymorphism in three racial groups
|
Matsutani, Akira
|
|
1992
|
13 |
3 |
p. 495-501
7 p.
|
artikel
|
| 50 |
Molecular characterization of cystic fibrosis: 16 Novel mutations identified by analysis of the whole cystic fibrosis conductance transmembrane regulator (CFTR) coding regions and splice site junctions
|
Fanen, Pascale
|
|
1992
|
13 |
3 |
p. 770-776
7 p.
|
artikel
|
| 51 |
Molecular cloning and chromosomal mapping of CCND genes encoding human D-type cyclins
|
Xiong, Yue
|
|
1992
|
13 |
3 |
p. 575-584
10 p.
|
artikel
|
| 52 |
Molecular linkage of the human CTLA4 and CD28 Ig-superfamily genes in yeast artificial chromosomes
|
Buonavista, Nathalie
|
|
1992
|
13 |
3 |
p. 856-861
6 p.
|
artikel
|
| 53 |
Molecular mapping of mouse chromosomes 4 and 6: Use of a flow-sorted robertsonian chromosome
|
Bahary, Nathan
|
|
1992
|
13 |
3 |
p. 761-769
9 p.
|
artikel
|
| 54 |
Molecular structure and genetic stability of human hypoxanthine phosphoribosyltransferase (HPRT) gene duplications
|
Monnat Jr., Raymond J.
|
|
1992
|
13 |
3 |
p. 788-796
9 p.
|
artikel
|
| 55 |
North Carolina macular dystrophy is assigned to chromosome 6
|
Small, Kent W.
|
|
1992
|
13 |
3 |
p. 681-685
5 p.
|
artikel
|
| 56 |
Nucleotide sequence analysis of human hypoxanthine phosphoribosyltransferase (HPRT) gene deletions
|
Monnat Jr., Raymond J.
|
|
1992
|
13 |
3 |
p. 777-787
11 p.
|
artikel
|
| 57 |
Ordering of human chromosome 3p markers by radiation hybrid mapping
|
Tamari, Mayumi
|
|
1992
|
13 |
3 |
p. 705-712
8 p.
|
artikel
|
| 58 |
Organization of the gene encoding the mouse T-cell-specific serine proteinase “granzyme A”
|
Ebnet, K.
|
|
1992
|
13 |
3 |
p. 502-508
7 p.
|
artikel
|
| 59 |
Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19q
|
Jansen, Gert
|
|
1992
|
13 |
3 |
p. 509-517
9 p.
|
artikel
|
| 60 |
Physical mapping and cloning of the proximal segment of the myotonic dystrophy gene region
|
Shutler, G.
|
|
1992
|
13 |
3 |
p. 518-525
8 p.
|
artikel
|
| 61 |
Refinement of diagnostic assays for a probable causal mutation for porcine and human malignant hyperthermia
|
Otsu, Kinya
|
|
1992
|
13 |
3 |
p. 835-837
3 p.
|
artikel
|
| 62 |
Regional localization of the gene for cardiac muscle actin (ACTC) on chromosome 15q
|
Kramer, P.L.
|
|
1992
|
13 |
3 |
p. 904-905
2 p.
|
artikel
|
| 63 |
Regional mapping of the human hepatocyte growth factor (HGF)-scatter factor gene to chromosome 7q21.1
|
Saccone, Salvatore
|
|
1992
|
13 |
3 |
p. 912-914
3 p.
|
artikel
|
| 64 |
Sequence analysis of a partial deletion of the human steroid sulfatase gene reveals 3 bp of homology at deletion breakpoints
|
Bernatowicz, Lynne F.
|
|
1992
|
13 |
3 |
p. 892-893
2 p.
|
artikel
|
| 65 |
Sequence, higher order repeat structure, and long-range organization of alpha satellite DNA specific to human chromosome 8
|
Ge, Ying
|
|
1992
|
13 |
3 |
p. 585-593
9 p.
|
artikel
|
| 66 |
Sequence of the human factor VIII-associated gene is conserved in mouse
|
Levinson, Barbara
|
|
1992
|
13 |
3 |
p. 862-865
4 p.
|
artikel
|
| 67 |
Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p
|
Guzzetta, Vito
|
|
1992
|
13 |
3 |
p. 551-559
9 p.
|
artikel
|
| 68 |
Structure and expression of the human p58clk-1 protein kinase chromosomal gene
|
Eipers, Peter G.
|
|
1992
|
13 |
3 |
p. 613-621
9 p.
|
artikel
|
| 69 |
Synteny between the loci for a novel FACIT-like collagen locus (D6S228E) and α1(IX) collagen (COL9A1) on 6q12–q14 in humans
|
Yoshioka, Hidekatsu
|
|
1992
|
13 |
3 |
p. 884-886
3 p.
|
artikel
|
| 70 |
The gene for receptor-linked protein-tyrosine-phosphatase (PTPA) is assigned to human chromosome 20p12-pter by in situ hybridization (ISH and FISH)
|
Rao, V.V.N. Gopal
|
|
1992
|
13 |
3 |
p. 906-907
2 p.
|
artikel
|
| 71 |
The β globin gene cluster of the prosimian primate Galago crassicaudatus: Nucleotide sequence determination of the 41-kb cluster and comparative sequence analyses
|
Tagle, Danilo A.
|
|
1992
|
13 |
3 |
p. 741-760
20 p.
|
artikel
|
| 72 |
The human IL-1 receptor antagonist gene (IL1RN) maps to chromosome 2q14–q21, in the region of the IL-1α and IL-1β loci
|
Steinkasserer, Alexander
|
|
1992
|
13 |
3 |
p. 654-657
4 p.
|
artikel
|
| 73 |
The human platelet-activating factor receptor gene (PTAFR) contains no introns and maps to chromosome 1
|
Seyfried, Christine E.
|
|
1992
|
13 |
3 |
p. 832-834
3 p.
|
artikel
|
| 74 |
The human β-subunit of rod photoreceptor cGMP phosphodiesterase: Complete retinal cDNA sequence and evidence for expression in brain
|
Collins, Colin
|
|
1992
|
13 |
3 |
p. 698-704
7 p.
|
artikel
|
| 75 |
The Machado-Joseph disease locus is different from the spinocerebellar ataxia locus (SCA1)
|
Carson, Wendy J.
|
|
1992
|
13 |
3 |
p. 852-855
4 p.
|
artikel
|
| 76 |
XY Sex reversal associated with a nonsense mutation in SRY
|
McElreavey, Ken D.
|
|
1992
|
13 |
3 |
p. 838-840
3 p.
|
artikel
|
| 77 |
YAC mapping by FISH using Alu-PCR-generated probes
|
Breen, Matthew
|
|
1992
|
13 |
3 |
p. 726-730
5 p.
|
artikel
|
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