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

J F Arena

Showing results (11-20 of 26) with videos related to

Pageof 3
Sort By:
American Journal of Medical Genetics|July 12, 1996
X-linked mental retardation with thin habitus, osteoporosis, and kyphoscoliosis: linkage to Xp21.3-p22.12J F Arena, C Schwartz, L Ouzts, et al.
American Journal of Medical Genetics|July 9, 1999
Gene for apparently nonsyndromic X-linked mental retardation (MRX32) maps to an 18-Mb region of Xp21.2-p22B Häne, R E Stevenson, J F Arena, et al.
American Journal of Medical Genetics|July 9, 1999
XLMR databaseD A Cabezas, J F Arena, R E Stevenson, et al.
Journal of Medical Genetics|June 1, 1997
Arch fingerprints, hypotonia, and areflexia associated with X linked mental retardationR E Stevenson, B Häne, J F Arena, et al.
ASDC Journal of Dentistry for Children|March 1, 1987
Orofacial manifestations of the Seckel syndromeL W Chilvarquer, V I dos Santos, M G Silva, et al.
Journal of Medical Genetics|September 9, 2000
A new X linked mental retardation (XLMR) syndrome with short stature, small testes, muscle wasting, and tremor localises to Xq24-q25D A Cabezas, R Slaugh, F Abidi, et al.
American Journal of Medical Genetics|April 1, 1992
Spastic paraplegia with iron deposits in the basal ganglia: a new X-linked mental retardation syndromeJ F Arena, C Schwartz, R Stevenson, et al.
Nature Genetics|November 14, 1997
A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivationR M Plenge, B D Hendrich, C Schwartz, et al.
American Journal of Medical Genetics|April 1, 1992
Allan-Herndon-Dudley syndrome: clinical and linkage studies on a second familyM G Bialer, L Lawrence, R E Stevenson, et al.
American Journal of Medical Genetics|July 9, 1999
X-linked mental retardation syndrome with seizures, hypogammaglobulinemia, and progressive gait disturbance is regionally mapped between xq21.33 and Xq23A E Chudley, D C Tackels, H A Lubs, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|July 12, 1996
X-linked mental retardation with thin habitus, osteoporosis, and kyphoscoliosis: linkage to Xp21.3-p22.12J F Arena, C Schwartz, L Ouzts, et al.
American Journal of Medical Genetics|July 9, 1999
Gene for apparently nonsyndromic X-linked mental retardation (MRX32) maps to an 18-Mb region of Xp21.2-p22B Häne, R E Stevenson, J F Arena, et al.
American Journal of Medical Genetics|July 9, 1999
XLMR databaseD A Cabezas, J F Arena, R E Stevenson, et al.
Journal of Medical Genetics|June 1, 1997
Arch fingerprints, hypotonia, and areflexia associated with X linked mental retardationR E Stevenson, B Häne, J F Arena, et al.
ASDC Journal of Dentistry for Children|March 1, 1987
Orofacial manifestations of the Seckel syndromeL W Chilvarquer, V I dos Santos, M G Silva, et al.
Journal of Medical Genetics|September 9, 2000
A new X linked mental retardation (XLMR) syndrome with short stature, small testes, muscle wasting, and tremor localises to Xq24-q25D A Cabezas, R Slaugh, F Abidi, et al.
American Journal of Medical Genetics|April 1, 1992
Spastic paraplegia with iron deposits in the basal ganglia: a new X-linked mental retardation syndromeJ F Arena, C Schwartz, R Stevenson, et al.
Nature Genetics|November 14, 1997
A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivationR M Plenge, B D Hendrich, C Schwartz, et al.
American Journal of Medical Genetics|April 1, 1992
Allan-Herndon-Dudley syndrome: clinical and linkage studies on a second familyM G Bialer, L Lawrence, R E Stevenson, et al.
American Journal of Medical Genetics|July 9, 1999
X-linked mental retardation syndrome with seizures, hypogammaglobulinemia, and progressive gait disturbance is regionally mapped between xq21.33 and Xq23A E Chudley, D C Tackels, H A Lubs, et al.
Pageof 3