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Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF

Journal of medical genetics, 2000-06, Vol.37 (6), p.446-448

2000

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Autosomal dominant polycystic kidney disease: Localization of the second gene to chromosome 4q13–q23

Genomics (San Diego, Calif.), 1993-12, Vol.18 (3), p.467-472

1993

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Genetic and Clinical Features of Sensorineural Hearing Loss Associated With the 1555 Mitochondrial Mutation

The Laryngoscope, 1997-04, Vol.107 (4), p.483-490

1997

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Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses

Human genetics, 2004-07, Vol.115 (2), p.128-138

2004

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Linkage heterogeneity of autosomal dominant polycystic kidney disease

The New England journal of medicine, 1988-10, Vol.319 (14), p.913-918

1988

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Linkage of usher syndrome type I gene (USH1B) to the long arm of chromosome 11

Genomics (San Diego, Calif.), 1992-12, Vol.14 (4), p.988-994

1992

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A Novel Locus for Autosomal Dominant Nonsyndromic Hearing Loss, DFNA13, Maps to Chromosome 6p

American journal of human genetics, 1997-10, Vol.61 (4), p.924-927

1997

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Autosomal-dominant, prelingual, nonprogressive sensorineural hearing loss: localization of the gene (DFNA8) to chromosome 11q by linkage in an Austrian family

Cytogenetic and genome research, 1998-01, Vol.82 (1-2), p.126-130

1998

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An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6

Genome research, 1995-10, Vol.5 (3), p.305-308

1995

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Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q

Human molecular genetics, 1995-09, Vol.4 (9), p.1643-1648

1995

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Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation

European journal of human genetics : EJHG, 1998-11, Vol.6 (6), p.563-569

1998

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Autosomal dominant branchio-oto-renal syndrome—localization of a disease gene to chromosome 8q by linkage in a Dutch family

Human molecular genetics, 1992-10, Vol.1 (7), p.491-495

1992

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Genetic Studies of Usher Syndrome

Annals of the New York Academy of Sciences, 1991-01, Vol.630 (1), p.167-175

1991

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Report on Attempts to Localize Usher Syndrome Type 1 by Linkage Analysis to Selected Candidate Regions

Annals of the New York Academy of Sciences, 1991-01, Vol.630 (1), p.298-300

1991

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Protides of the Mustelidae: immunoresponse of mustelids to Aleutian mink disease virus

American journal of veterinary research, 1978-06, Vol.39 (6), p.1011

1978

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Comparison of cavity preparation quality using an electric motor handpiece and an air turbine dental handpiece

The Journal of the American Dental Association (1939), 2005-08, Vol.136 (8), p.1101-1105

2005

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Stable accelerometer attachment to the skin surface

The Journal of prosthetic dentistry, 2005-11, Vol.94 (5), p.466-467

2005

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Simple technique for cleaning and drying the barrel of a plastic impression syringe

The Journal of prosthetic dentistry, 2005-08, Vol.94 (2), p.199-199

2005

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Simple instrument for auscultation of temporomandibular joint sounds

The Journal of prosthetic dentistry, 2004-12, Vol.92 (6), p.604-604

2004

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Easily fabricated rotary margin burnisher

The Journal of prosthetic dentistry, 2005, Vol.93 (1), p.97-97

2005

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Genetic linkage studies of autosomal dominant polycystic kidney disease : search for the second gene in a large Sicilian family

Human genetics, 1991-06, Vol.87 (2), p.129-133

1991

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Simple instrument for detecting minor differences in surface texture

The Journal of prosthetic dentistry, 2004-03, Vol.91 (3), p.298-298

2004

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Voting at the S.R.M

BMJ, 1965-10, Vol.2 (5466), p.883-883

1965

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PREVALENCE OF Pharurus pallasii IN THE BELUGA WHALE (Delphinapterus leucas) OF CHURCHILL RIVER BASIN, MANITOBA

Journal of wildlife diseases, 1977-10, Vol.13 (4), p.338-340

1977

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The last sources of Roman history, 44 B.C. -A.D. 68

Kenyon, J B

1968

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Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF

Autosomal dominant polycystic kidney disease: Localization of the second gene to chromosome 4q13–q23

Genetic and Clinical Features of Sensorineural Hearing Loss Associated With the 1555 Mitochondrial Mutation

Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses

Linkage heterogeneity of autosomal dominant polycystic kidney disease

Linkage of usher syndrome type I gene (USH1B) to the long arm of chromosome 11

A Novel Locus for Autosomal Dominant Nonsyndromic Hearing Loss, DFNA13, Maps to Chromosome 6p

Autosomal-dominant, prelingual, nonprogressive sensorineural hearing loss: localization of the gene (DFNA8) to chromosome 11q by linkage in an Austrian family

An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6

Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q

Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation

Autosomal dominant branchio-oto-renal syndrome—localization of a disease gene to chromosome 8q by linkage in a Dutch family

Genetic Studies of Usher Syndrome

Report on Attempts to Localize Usher Syndrome Type 1 by Linkage Analysis to Selected Candidate Regions

Protides of the Mustelidae: immunoresponse of mustelids to Aleutian mink disease virus

Comparison of cavity preparation quality using an electric motor handpiece and an air turbine dental handpiece

Stable accelerometer attachment to the skin surface

Simple technique for cleaning and drying the barrel of a plastic impression syringe

Simple instrument for auscultation of temporomandibular joint sounds

Easily fabricated rotary margin burnisher

Genetic linkage studies of autosomal dominant polycystic kidney disease : search for the second gene in a large Sicilian family

Simple instrument for detecting minor differences in surface texture

Voting at the S.R.M

PREVALENCE OF Pharurus pallasii IN THE BELUGA WHALE (Delphinapterus leucas) OF CHURCHILL RIVER BASIN, MANITOBA

The last sources of Roman history, 44 B.C. -A.D. 68

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