-
Integration of Ecogpt and SV40 early region sequences into human chromosome 17: a dominant selection system in whole cell and microcell human-mouse hybrids.
EMBO J. 1983;2(9):1577-84
PMID: 11892815
-
Human DNA sequences homologous to a protein coding region conserved between homeotic genes of Drosophila.
Cell. 1984 Oct;38(3):667-73
PMID: 6091895
-
Differential Giemsa staining of sister chromatids and the study of chromatid exchanges without autoradiography.
Chromosoma. 1974;48(4):341-53
PMID: 4141298
-
Detection of specific sequences among DNA fragments separated by gel electrophoresis.
J Mol Biol. 1975 Nov 5;98(3):503-17
PMID: 1195397
-
Further evidence for a non-random chromosomal abnormality in acute promyelocytic leukemia.
Int J Cancer. 1977 Dec 15;20(6):869-72
PMID: 271143
-
Phenotype stabilisation and integration of transferred material in chromosome-mediated gene transfer.
Nature. 1979 Aug 23;280(5724):657-60
PMID: 471042
-
Localization of single copy DNA sequences of G-banded human chromosomes by in situ hybridization.
Chromosoma. 1981;83(3):431-9
PMID: 7273954
-
Chromosomal localization of the human placental lactogen-growth hormone gene cluster to 17q22-24.
Am J Hum Genet. 1982 Mar;34(2):227-34
PMID: 7072716
-
Human type I procollagen genes are located on different chromosomes.
Proc Natl Acad Sci U S A. 1982 Nov;79(21):6627-30
PMID: 6292910
-
A monoclonal antibody recognizing a cell surface antigen coded for by a gene on human chromosome 17.
Ann Hum Genet. 1982 Oct;46(Pt 4):337-47
PMID: 6984317
-
Genetic analysis of the 15;17 chromosome translocation associated with acute promyelocytic leukemia.
Proc Natl Acad Sci U S A. 1983 Aug;80(16):5007-11
PMID: 6576373
-
Multigene family for sarcomeric myosin heavy chain in mouse and human DNA: localization on a single chromosome.
Science. 1983 Aug 19;221(4612):766-9
PMID: 6879174
-
Isolation and characterization of multiple human genes homologous to the oncogenes of avian erythroblastosis virus.
EMBO J. 1983;2(4):561-5
PMID: 6313346
-
High-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization.
Proc Natl Acad Sci U S A. 1983 Nov;80(22):6932-6
PMID: 6196780
-
Direct isolation of the functional human thymidine kinase gene with a cosmid shuttle vector.
Proc Natl Acad Sci U S A. 1984 Jan;81(2):414-8
PMID: 6320187
-
DNA polymorphic loci mapped to human chromosomes 3, 5, 9, 11, 17, 18, and 22.
Proc Natl Acad Sci U S A. 1984 Apr;81(8):2447-51
PMID: 6585809
-
"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.
Anal Biochem. 1984 Feb;137(1):266-7
PMID: 6329026
-
New chromosomal syndrome: Miller-Dieker syndrome and monosomy 17p13.
Hum Genet. 1984;67(2):193-200
PMID: 6745939
-
DNA and chromatin structure of the human alpha 1 (I) collagen gene.
J Biol Chem. 1984 Dec 10;259(23):14906-13
PMID: 6094581
-
Isolation and characterization of a human p53 cDNA clone: expression of the human p53 gene.
EMBO J. 1984 Dec 20;3(13):3257-62
PMID: 6396087
-
Human genes for U2 small nuclear RNA map to a major adenovirus 12 modification site on chromosome 17.
Nature. 1985 Mar 7-13;314(6006):115-6
PMID: 2579339
-
Chromosomal assignments of the genes coding for human types II, III, and IV collagen: a dispersed gene family.
Proc Natl Acad Sci U S A. 1985 May;82(10):3330-4
PMID: 2987919
-
Molecular cloning and expression of cDNA for human granulocyte colony-stimulating factor.
Nature. 1986 Jan 30-Feb 5;319(6052):415-8
PMID: 3484805
-
The nerve growth factor receptor gene is at human chromosome region 17q12-17q22, distal to the chromosome 17 breakpoint in acute leukemias.
Proc Natl Acad Sci U S A. 1986 Mar;83(5):1403-7
PMID: 3006050
-
Development of new methods in human gene mapping: selection for fragments of the human Y chromosome after chromosome-mediated gene transfer.
EMBO J. 1986 May;5(5):979-85
PMID: 3720729
-
The gene encoding the large subunit of human RNA polymerase II is located on the short arm of chromosome 17.
Am J Hum Genet. 1986 Jun;38(6):812-8
PMID: 3460332
-
Interstitial deletion of (17)(p11.2p11.2) in nine patients.
Am J Med Genet. 1986 Jul;24(3):393-414
PMID: 2425619
-
Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.
Am J Med Genet. 1986 Jul;24(3):421-32
PMID: 3728561
-
Localization of a beta-crystallin gene, Hu beta A3/A1 (gene symbol: CRYB1), to the long arm of human chromosome 17.
Cytogenet Cell Genet. 1986;42(4):202-7
PMID: 3757553
-
Studies on the expression of an H-2K/human growth hormone fusion gene in giant transgenic mice.
EMBO J. 1986 Aug;5(8):1877-83
PMID: 3019667
-
Human myeloperoxidase gene: molecular cloning and expression in leukemic cells.
Blood. 1986 Dec;68(6):1411-4
PMID: 3022847
-
Structure, organization, and sequence of alpha satellite DNA from human chromosome 17: evidence for evolution by unequal crossing-over and an ancestral pentamer repeat shared with the human X chromosome.
Mol Cell Biol. 1986 Sep;6(9):3156-65
PMID: 3785225
-
Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17.
Science. 1987 May 29;236(4805):1100-2
PMID: 3107130
-
HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13.
Proc Natl Acad Sci U S A. 1987 Aug;84(15):5355-9
PMID: 3037545
-
Investigation of chromosome-mediated gene transfer using the HPRT region of the human X chromosome as a model.
Genes Dev. 1987 Apr;1(2):172-8
PMID: 3678822
-
A centromere-based linkage group on the long arm of human chromosome 17.
Cytogenet Cell Genet. 1988;47(1-2):109-10
PMID: 3162714
-
Regional mapping panel for human chromosome 17: application to neurofibromatosis type 1.
Genomics. 1987 Dec;1(4):374-81
PMID: 3130306
-
Proceedings: Regional localization of the human genes for thymidine kinase, lactate dehydrogenase-A, and esterase-A.
Cytogenet Cell Genet. 1974;13(1):108-10
PMID: 4827473