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

R M Winter

Showing results (141-150 of 219) with videos related to

Pageof 22
Sort By:
Journal of Medical Genetics|December 14, 1999
Popliteal pterygium syndrome: a clinical study of three families and report of linkage to the Van der Woude syndrome locus on 1q32M M Lees, R M Winter, S Malcolm, et al.
Clinical Dysmorphology|April 18, 1998
Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome)J Amiel, P M Watkin, M Tassabehji, et al.
Journal of Medical Genetics|June 1, 1992
Confirmation of an association between RFLPs at the transforming growth factor-alpha locus and non-syndromic cleft lip and palateS E Holder, G M Vintiner, B Farren, et al.
Clinical Dysmorphology|April 20, 2001
Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delayB B de Vries, W G van'tHoff, R A Surtees, et al.
Human Molecular Genetics|July 1, 1997
The oral-facial-digital syndrome type 1 (OFD1), a cause of polycystic kidney disease and associated malformations, maps to Xp22.2-Xp22.3S A Feather, A S Woolf, D Donnai, et al.
Progress in Clinical and Biological Research|January 1, 1981
The analysis of spontaneous abortion using a new half-sib model for qualitative traitsW L Golden, R M Winter, L Eaves, et al.
Clinical Dysmorphology|January 1, 1993
Previously unrecognized form of familial spondyloepiphyseal dysplasia tarda with characteristic faciesS M Huson, S Crowley, C M Hall, et al.
Journal of Medical Genetics|April 1, 1984
The 3-M syndromeR M Winter, M Baraitser, D B Grant, et al.
Clinical Genetics|August 16, 2003
ROR2 is mutated in hereditary brachydactyly with nail dysplasia, but not in Sorsby syndromeC Bacchelli, L C Wilson, J A Cook, et al.
Journal of Medical Genetics|March 1, 1994
Crouzon syndrome is not linked to craniosynostosis loci at 7p and 5qterW Reardon, L van Herwerden, C Rose, et al.
Pageof 22

Showing results (141-150 of 219) with videos related to

Sort By:
Pageof 22
Journal of Medical Genetics|December 14, 1999
Popliteal pterygium syndrome: a clinical study of three families and report of linkage to the Van der Woude syndrome locus on 1q32M M Lees, R M Winter, S Malcolm, et al.
Clinical Dysmorphology|April 18, 1998
Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome)J Amiel, P M Watkin, M Tassabehji, et al.
Journal of Medical Genetics|June 1, 1992
Confirmation of an association between RFLPs at the transforming growth factor-alpha locus and non-syndromic cleft lip and palateS E Holder, G M Vintiner, B Farren, et al.
Clinical Dysmorphology|April 20, 2001
Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delayB B de Vries, W G van'tHoff, R A Surtees, et al.
Human Molecular Genetics|July 1, 1997
The oral-facial-digital syndrome type 1 (OFD1), a cause of polycystic kidney disease and associated malformations, maps to Xp22.2-Xp22.3S A Feather, A S Woolf, D Donnai, et al.
Progress in Clinical and Biological Research|January 1, 1981
The analysis of spontaneous abortion using a new half-sib model for qualitative traitsW L Golden, R M Winter, L Eaves, et al.
Clinical Dysmorphology|January 1, 1993
Previously unrecognized form of familial spondyloepiphyseal dysplasia tarda with characteristic faciesS M Huson, S Crowley, C M Hall, et al.
Journal of Medical Genetics|April 1, 1984
The 3-M syndromeR M Winter, M Baraitser, D B Grant, et al.
Clinical Genetics|August 16, 2003
ROR2 is mutated in hereditary brachydactyly with nail dysplasia, but not in Sorsby syndromeC Bacchelli, L C Wilson, J A Cook, et al.
Journal of Medical Genetics|March 1, 1994
Crouzon syndrome is not linked to craniosynostosis loci at 7p and 5qterW Reardon, L van Herwerden, C Rose, et al.
Pageof 22