Pairwise linkage analysis of 11 loci on human chromosome 4.

Construction of a genetic linkage map in man using restriction fragment length polymorphisms.

1980 • 8,270 citations

Strategies for multilocus linkage analysis in humans.

1984 • 2,600 citations

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

1983 • 1,952 citations

Sequential tests for the detection of linkage.

1955 • 1,590 citations

γ-Interferon transcriptionally regulates an early-response gene containing homology to platelet proteins

1985 • 949 citations

Cloning the gene for an inherited human disorder—chronic granulomatous disease—on the basis of its chromosomal location

1986 • 839 citations

A deletion in chromosome 22 can cause digeorge syndrome

1981 • 366 citations

Loss of a Harvey ras allele in sporadic Wilms' tumour

1984 • 336 citations

Construction of linkage maps with DNA markers for human chromosomes

1985 • 325 citations

Molecular structure of the human albumin gene is revealed by nucleotide sequence within q11-22 of chromosome 4.

1986 • 297 citations

Evolution and organization of the fibrinogen locus on chromosome 4: gene duplication accompanied by transposition and inversion.

1985 • 268 citations

Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases.

1982 • 238 citations

Hu- ets -1 and Hu- ets -2 Genes Are Transposed in Acute Leukemias with (4;11) and (8;21) Translocations

1986 • 191 citations

Characterization of a complementary deoxyribonucleic acid coding for the .gamma. chain of human fibrinogen

1983 • 132 citations

Characterization of complementary deoxyribonucleic acid and genomic deoxyribonucleic acid for the .beta. chain of human fibrinogen

1983 • 126 citations

Interferon-inducible gene maps to a chromosomal band associated with a (4;11) translocation in acute leukemia cells.

1987 • 100 citations

Gene for T-Cell Growth Factor: Location on Human Chromosome 4q and Feline Chromosome B1

1984 • 97 citations

Linkage of the evolutionarily-related serum albumin and alpha-fetoprotein genes within q11-22 of human chromosome 4.

1983 • 95 citations

Tandem arrangement of the albumin and α-fetoprotein genes in the human genome

1984 • 88 citations

Multipoint gene mapping using seriation. I. General methods.

1987 • 82 citations

Linkage disequilibrium and evolutionary relationships of DNA variants (restriction enzyme fragment length polymorphisms) at the serum albumin locus.

1984 • 79 citations

Determination of the DNA content of human chromosomes by flow cytometry

1986 • 73 citations

Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia.

1983 • 67 citations

Report of the committee on the genetic constitution of chromosomes 3 and 4

1985 • 58 citations

Linkage between dentinogenesis imperfecta and Gc

1982 • 56 citations

Human genes for insulin-like growth factors I and II and epidermal growth factor are located on 12q22→q24.1, 11p15, and 4q25→q27, respectively

1986 • 49 citations

Linkage of GLO with HLA and Bf. Effect of Population and Sex on Recombination Frequency*

1976 • 48 citations

Interstitial deletion 4q and Rieger syndrome

1981 • 44 citations

Chromosomal localization of human and rat Aα, Bβ, and γ fibrinogen genes by in situ hybridization

1986 • 37 citations

A Source Book for Linkage in Man

1979 • 34 citations

The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic markers

1984 • 33 citations

The identification of a DNA polymorphism of the ? fibrinogen gene, and the regional assignment of the human fibrinogen genes to 4q26-qter

1984 • 32 citations

Fibrinogen γ chain locus is on chromosome 4 in man

1982 • 30 citations

RELPs for epidermal growth factor (EGF), a single copy sequence at 4q25-4q27

1986 • 20 citations

Chromosomal localization of group-specific component by in situ hybridization

1986 • 17 citations

Linkage studies between polymorphic markers on chromosome 4 and cystic fibrosis

1985 • 16 citations

Human metallothionein-II processed gene is located in region p11→q21 of chromosome 4

1985 • 13 citations

Anterior segment mesenchymal dysgenesis: probable linkage to the MNS blood group on chromosome 4.

1982 • 13 citations

Close linkage of <i>MT2P1 </i>with <i>GC </i>on chromosome 4

1986 • 13 citations

A frequent restriction fragment length polymorphism in the human metallothionein-II processed gene region is evolutionarily conserved.

1984 • 12 citations

Molecular biology of interleukin 2

1985 • 9 citations

RFLPs for the human alphafetoprotein(AFP), at 4q11-4q13

1985 • 5 citations