Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

H Asher

Showing results (21-30 of 46) with videos related to

Pageof 5
Sort By:
American Journal of Medical Genetics|August 8, 1997
Autosomal dominant microcephaly with normal intelligence, short palpebral fissures, and digital anomaliesJ W Innis, J H Asher, A K Poznanski, et al.
Journal of Medical Genetics|June 1, 1997
The incidence of deafness is non-randomly distributed among families segregating for Waardenburg syndrome type 1 (WS1)R Morell, T B Friedman, J H Asher, et al.
Dental Clinics of North America|March 21, 2017
Role of Oral Microbial Infections in Oral CancerBrett L Ferguson, Scott Barber, Imani H Asher, et al.
Journal of Medical Genetics|April 16, 1998
Septo-optic dysplasia and WS1 in the proband of a WS1 family segregating for a novel mutation in PAX3 exon 7M L Carey, T B Friedman, J H Asher, et al.
Human Molecular Genetics|July 11, 1992
A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian familyR Morell, T B Friedman, S Moeljopawiro, et al.
Gene|January 15, 1997
Human inner ear OCP2 cDNA maps to 5q22-5q35.2 with related sequences on chromosomes 4p16.2-4p14, 5p13-5q22, 7pter-q22, 10 and 12p13-12qterY Liang, H Chen, J H Asher, et al.
Human Heredity|January 1, 1997
Three mutations in the paired homeodomain of PAX3 that cause Waardenburg syndrome type 1R Morell, M L Carey, A K Lalwani, et al.
Laboratory Animal Science|May 20, 1999
Auditory brainstem responses in Golden Syrian hamsters (Mesocricetus auratus) affected with the Wh geneG K Amedofu, K V Gopal, J H Asher, et al.
Human Molecular Genetics|January 1, 1993
A highly informative dinucleotide repeat polymorphism at the D2S211 locus linked to ALPP, FN1 and TNP1T D Barber, R Morell, D H Johnson, et al.
Genomics|June 15, 1996
Effects of Pax3 modifier genes on craniofacial morphology, pigmentation, and viability: a murine model of Waardenburg syndrome variationJ H Asher, R W Harrison, R Morell, et al.
Pageof 5

Showing results (21-30 of 46) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|August 8, 1997
Autosomal dominant microcephaly with normal intelligence, short palpebral fissures, and digital anomaliesJ W Innis, J H Asher, A K Poznanski, et al.
Journal of Medical Genetics|June 1, 1997
The incidence of deafness is non-randomly distributed among families segregating for Waardenburg syndrome type 1 (WS1)R Morell, T B Friedman, J H Asher, et al.
Dental Clinics of North America|March 21, 2017
Role of Oral Microbial Infections in Oral CancerBrett L Ferguson, Scott Barber, Imani H Asher, et al.
Journal of Medical Genetics|April 16, 1998
Septo-optic dysplasia and WS1 in the proband of a WS1 family segregating for a novel mutation in PAX3 exon 7M L Carey, T B Friedman, J H Asher, et al.
Human Molecular Genetics|July 11, 1992
A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian familyR Morell, T B Friedman, S Moeljopawiro, et al.
Gene|January 15, 1997
Human inner ear OCP2 cDNA maps to 5q22-5q35.2 with related sequences on chromosomes 4p16.2-4p14, 5p13-5q22, 7pter-q22, 10 and 12p13-12qterY Liang, H Chen, J H Asher, et al.
Human Heredity|January 1, 1997
Three mutations in the paired homeodomain of PAX3 that cause Waardenburg syndrome type 1R Morell, M L Carey, A K Lalwani, et al.
Laboratory Animal Science|May 20, 1999
Auditory brainstem responses in Golden Syrian hamsters (Mesocricetus auratus) affected with the Wh geneG K Amedofu, K V Gopal, J H Asher, et al.
Human Molecular Genetics|January 1, 1993
A highly informative dinucleotide repeat polymorphism at the D2S211 locus linked to ALPP, FN1 and TNP1T D Barber, R Morell, D H Johnson, et al.
Genomics|June 15, 1996
Effects of Pax3 modifier genes on craniofacial morphology, pigmentation, and viability: a murine model of Waardenburg syndrome variationJ H Asher, R W Harrison, R Morell, et al.
Pageof 5