C W Cremers|S J Geerts - JoVE Visualize

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Nature Genetics|March 18, 1999

Heterozygous mutations in the gene encoding noggin affect human joint morphogenesisY Gong, D Krakow, J Marcelino, et al.

Genomics|April 1, 1997

Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1pG Van Camp, P J Coucke, H Kunst, et al.

American Journal of Human Genetics|November 4, 2000

Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type IL M Astuto, M D Weston, C A Carney, et al.

Human Molecular Genetics|June 9, 1998

Two frequent missense mutations in Pendred syndromeP Van Hauwe, L A Everett, P Coucke, et al.

Human Molecular Genetics|September 1, 1996

Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4Y J de Kok, E R Vossenaar, C W Cremers, et al.

Human Molecular Genetics|June 17, 1999

Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 familiesP J Coucke, P Van Hauwe, P M Kelley, et al.

Nature Genetics|December 2, 1999

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)W T McGuirt, S D Prasad, A J Griffith, et al.

Nature Genetics|January 23, 1999

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafnessF E Karet, K E Finberg, R D Nelson, et al.

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Showing results (151-160 of 158) with videos related to

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You have reached the last page of results.This site can display upto 158 results.

Nature Genetics|March 18, 1999

Heterozygous mutations in the gene encoding noggin affect human joint morphogenesisY Gong, D Krakow, J Marcelino, et al.

Genomics|April 1, 1997

Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1pG Van Camp, P J Coucke, H Kunst, et al.

American Journal of Human Genetics|November 4, 2000

Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type IL M Astuto, M D Weston, C A Carney, et al.

Human Molecular Genetics|June 9, 1998

Two frequent missense mutations in Pendred syndromeP Van Hauwe, L A Everett, P Coucke, et al.

Human Molecular Genetics|September 1, 1996

Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4Y J de Kok, E R Vossenaar, C W Cremers, et al.

Human Molecular Genetics|June 17, 1999

Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 familiesP J Coucke, P Van Hauwe, P M Kelley, et al.

Nature Genetics|December 2, 1999

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)W T McGuirt, S D Prasad, A J Griffith, et al.

Nature Genetics|January 23, 1999

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafnessF E Karet, K E Finberg, R D Nelson, et al.

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