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R F Mueller

Showing results (61-70 of 85) with videos related to

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Clinical Genetics|April 19, 2003
The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UKD C Blaydon, R F Mueller, T P Hutchin, et al.
American Journal of Human Genetics|March 21, 2000
A third novel locus for primary autosomal recessive microcephaly maps to chromosome 9q34L Moynihan, A P Jackson, E Roberts, et al.
American Journal of Medical Genetics|July 1, 1994
Six cases of 7p deletion: clinical, cytogenetic, and molecular studiesK A Chotai, L A Brueton, L van Herwerden, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
A gene for ataxic cerebral palsy maps to chromosome 9p12-q12D P McHale, A P Jackson, Campbell, et al.
British Journal of Anaesthesia|January 1, 1993
Genetic linkage analysis of chromosome 19 markers in malignant hyperthermiaS P Ball, H R Dorkins, F R Ellis, et al.
Journal of Medical Genetics|November 1, 1989
Diagnostic and counselling difficulties using a fully comprehensive screening protocol for families at risk for tuberous sclerosisL I al-Gazali, R J Arthur, J T Lamb, et al.
American Journal of Human Genetics|February 11, 1999
A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25D P McHale, S Mitchell, S Bundey, et al.
Archives of Otolaryngology--Head & Neck Surgery|January 24, 1998
Presymptomatic diagnosis of nonsyndromic hearing loss by genotypingA H Chen, R F Mueller, S D Prasad, et al.
Clinical Dysmorphology|November 14, 1997
Macrocephaly with cutis marmorata, haemangioma and syndactyly--a distinctive overgrowth syndromeJ Clayton-Smith, B Kerr, H Brunner, et al.
Journal of Medical Genetics|September 9, 2000
A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairmentT P Hutchin, M J Parker, I D Young, et al.
Pageof 9

Showing results (61-70 of 85) with videos related to

Sort By:
Pageof 9
Clinical Genetics|April 19, 2003
The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UKD C Blaydon, R F Mueller, T P Hutchin, et al.
American Journal of Human Genetics|March 21, 2000
A third novel locus for primary autosomal recessive microcephaly maps to chromosome 9q34L Moynihan, A P Jackson, E Roberts, et al.
American Journal of Medical Genetics|July 1, 1994
Six cases of 7p deletion: clinical, cytogenetic, and molecular studiesK A Chotai, L A Brueton, L van Herwerden, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
A gene for ataxic cerebral palsy maps to chromosome 9p12-q12D P McHale, A P Jackson, Campbell, et al.
British Journal of Anaesthesia|January 1, 1993
Genetic linkage analysis of chromosome 19 markers in malignant hyperthermiaS P Ball, H R Dorkins, F R Ellis, et al.
Journal of Medical Genetics|November 1, 1989
Diagnostic and counselling difficulties using a fully comprehensive screening protocol for families at risk for tuberous sclerosisL I al-Gazali, R J Arthur, J T Lamb, et al.
American Journal of Human Genetics|February 11, 1999
A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25D P McHale, S Mitchell, S Bundey, et al.
Archives of Otolaryngology--Head & Neck Surgery|January 24, 1998
Presymptomatic diagnosis of nonsyndromic hearing loss by genotypingA H Chen, R F Mueller, S D Prasad, et al.
Clinical Dysmorphology|November 14, 1997
Macrocephaly with cutis marmorata, haemangioma and syndactyly--a distinctive overgrowth syndromeJ Clayton-Smith, B Kerr, H Brunner, et al.
Journal of Medical Genetics|September 9, 2000
A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairmentT P Hutchin, M J Parker, I D Young, et al.
Pageof 9