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Was the Human Genome Project worth the effort?

American journal of ophthalmology, 2005-09, Vol.140 (3), p.568-568

Daiger, S.P.

2005

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Localization of two genes for usher syndrome type I to chromosome 11

Genomics (San Diego, Calif.), 1992-12, Vol.14 (4), p.995-1002

1992

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Human Glutamate Pyruvate Transaminase (GPT): Localization to 8q24.3, cDNA and Genomic Sequences, and Polymorphic Sites

Genomics (San Diego, Calif.), 1997-03, Vol.40 (2), p.247-252

1997

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Nonsyndromic cleft lip and palate : no evidence of linkage to HLA or factor 13A

American journal of human genetics, 1993-06, Vol.52 (6), p.1230-1233

1993

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Localization and Characterization of the Human ADP-Ribosylation Factor 5 (ARF5) Gene

Genomics (San Diego, Calif.), 1997-05, Vol.41 (3), p.481-484

1997

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Evidence for genetic heterogeneity in tuberous sclerosis : one locus on chromosome 9 and at least one locus elsewhere

American journal of human genetics, 1992-10, Vol.51 (4), p.709-720

1992

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Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis. Nat Gen 2000;24:79–83

American journal of ophthalmology, 2000-06, Vol.129 (6), p.834-835

2000

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A new Sty l RFLP and haplotypes with the Hin dIII RFLP at the D8S5 (TL11) locus

Nucleic acids research, 1991, Vol.19 (17), p.4790-4790

1991

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Dinucleotide repeat polymorphism at the human tissue plasminogen activator gene (PLAT)

Nucleic acids research, 1991-11, Vol.19 (21), p.6058-6058

1991

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Tetranucleotide repeat polymorphism (D8S582) for human EST00680 (D8S340E)

Human molecular genetics, 1994-02, Vol.3 (2), p.386-386

1994

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The human apolipoprotein B-100 gene: A highly polymorphic gene that maps to the short arm of chromosome 2

Biochemical and biophysical research communications, 1985-11, Vol.133 (1), p.248-255

1985

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Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysis

American journal of medical genetics, 1994-06, Vol.51 (2), p.176-184

1994

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Further evidence of exclusion of linkage between type II autosomal dominant retinitis pigmentosa (ADRP) and D3S47 on 3q

Genomics (San Diego, Calif.), 1990-09, Vol.8 (1), p.179-181

1990

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A new StyI RFLP and haplotypes with the HindIII RFLP at the D8S5 (TL 11) locus

Nucleic acids research, 1991-09, Vol.19 (17), p.4790-4790

1991

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Exclusion of Usher syndrome gene from much of chromosome 4

Cytogenetic and genome research, 1989-01, Vol.50 (2-3), p.102-106

1989

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A tight linkage cluster, with two new RFLPs (D8S96 and D8S108), in the interval 8cen-q13

Nucleic acids research, 1992-03, Vol.20 (6), p.1426-1426

1992

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Linkage analysis of human chromosome 4: exclusion of autosomal dominant retinitis pigmentosa (ADRP) and detection of new linkage groups

Cytogenetic and genome research, 1989-01, Vol.50 (4), p.181-187

1989

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Assignment of autosomal dominant spinocerebellar ataxia centromeric to HLA using multilocus linkage analysis

Human immunology, 1988, Vol.23 (2), p.161-161

1988

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Was the Human Genome Project worth the effort?

Localization of two genes for usher syndrome type I to chromosome 11

Human Glutamate Pyruvate Transaminase (GPT): Localization to 8q24.3, cDNA and Genomic Sequences, and Polymorphic Sites

Nonsyndromic cleft lip and palate : no evidence of linkage to HLA or factor 13A

Localization and Characterization of the Human ADP-Ribosylation Factor 5 (ARF5) Gene

Evidence for genetic heterogeneity in tuberous sclerosis : one locus on chromosome 9 and at least one locus elsewhere

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis. Nat Gen 2000;24:79–83

A new Sty l RFLP and haplotypes with the Hin dIII RFLP at the D8S5 (TL11) locus

Dinucleotide repeat polymorphism at the human tissue plasminogen activator gene (PLAT)

Tetranucleotide repeat polymorphism (D8S582) for human EST00680 (D8S340E)

The human apolipoprotein B-100 gene: A highly polymorphic gene that maps to the short arm of chromosome 2

Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysis

Further evidence of exclusion of linkage between type II autosomal dominant retinitis pigmentosa (ADRP) and D3S47 on 3q

A new StyI RFLP and haplotypes with the HindIII RFLP at the D8S5 (TL 11) locus

Exclusion of Usher syndrome gene from much of chromosome 4

A tight linkage cluster, with two new RFLPs (D8S96 and D8S108), in the interval 8cen-q13

Linkage analysis of human chromosome 4: exclusion of autosomal dominant retinitis pigmentosa (ADRP) and detection of new linkage groups

Assignment of autosomal dominant spinocerebellar ataxia centromeric to HLA using multilocus linkage analysis

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