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

S Joss

Showing results (1-10 of 8) with videos related to

Pageof 1
Sort By:
British Journal of Plastic Surgery|May 1, 1990
Tissue expansion technique and the transposition flapG S Joss, N Zoltie, P Chapman
Clinical and Experimental Dermatology|January 31, 2019
Inherited desmoplastic trichoepitheliomasM-L Lovgren, N Rajan, S Joss, et al.
Clinical Genetics|April 16, 2003
De novo translocation (1; 2)(q32; p25) associated with bilateral renal dysplasiaS Joss, A Howatson, A Trainer, et al.
Journal of Medical Genetics|July 4, 2006
A nonsense mutation in the first transmembrane domain of connexin 43 underlies autosomal recessive oculodentodigital syndromeR J Richardson, S Joss, S Tomkin, et al.
European Journal of Human Genetics : EJHG|June 16, 2019
De novo variants in CNOT3 cause a variable neurodevelopmental disorderR Martin, M Splitt, D Genevieve, et al.
Human Genetics|December 12, 2013
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndromeR S Møller, L R Jensen, S M Maas, et al.
Cell Death and Differentiation|July 23, 2016
ASPP2 deficiency causes features of 1q41q42 microdeletion syndromeJ Zak, V Vives, D Szumska, et al.
Molecular Psychiatry|August 24, 2016
De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and femalesE E Palmer, T Stuhlmann, S Weinert, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
British Journal of Plastic Surgery|May 1, 1990
Tissue expansion technique and the transposition flapG S Joss, N Zoltie, P Chapman
Clinical and Experimental Dermatology|January 31, 2019
Inherited desmoplastic trichoepitheliomasM-L Lovgren, N Rajan, S Joss, et al.
Clinical Genetics|April 16, 2003
De novo translocation (1; 2)(q32; p25) associated with bilateral renal dysplasiaS Joss, A Howatson, A Trainer, et al.
Journal of Medical Genetics|July 4, 2006
A nonsense mutation in the first transmembrane domain of connexin 43 underlies autosomal recessive oculodentodigital syndromeR J Richardson, S Joss, S Tomkin, et al.
European Journal of Human Genetics : EJHG|June 16, 2019
De novo variants in CNOT3 cause a variable neurodevelopmental disorderR Martin, M Splitt, D Genevieve, et al.
Human Genetics|December 12, 2013
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndromeR S Møller, L R Jensen, S M Maas, et al.
Cell Death and Differentiation|July 23, 2016
ASPP2 deficiency causes features of 1q41q42 microdeletion syndromeJ Zak, V Vives, D Szumska, et al.
Molecular Psychiatry|August 24, 2016
De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and femalesE E Palmer, T Stuhlmann, S Weinert, et al.
Pageof 1