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Publications by Nel T. Tijmes
A Gene for X-Linked Optic Atrophy Is Closely Linked to the Xp11.4-Xp11.2 Region of the X Chromosome
American Journal of Human Genetics
Genetics
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New Distal Marker Closely Linked to the Fragile X Locus
Human Genetics
Genetics
Multiple in Vivo Footprints Are Specific to the Active Allele of the X-Linked Human Hypoxanthine Phosphoribosyltransferase Gene 5' Region: Implications for X Chromosome Inactivation.
Molecular and Cellular Biology
Cell Biology
Molecular Biology
A De Novo Missense Mutation in a Critical Domain of the X-Linked DDP Gene Causes the Typical Deafness–dystonia–optic Atrophy Syndrome
European Journal of Human Genetics
Genetics
A Gene for Pachyonychia Congenita Is Closely Linked to the Keratin Gene Cluster on 17q12-Q21.
Journal of Medical Genetics
Genetics
A Family With Apparently Sex-Linked Optic Atrophy.
Journal of Medical Genetics
Genetics
A New Chromosome X Exon-Specific Microarray Platform for Screening of Patients With X-Linked Disorders
Journal of Molecular Diagnostics
Forensic Medicine
Pathology
Molecular Medicine
X-Linked Agammaglobulinemia
X-Linked Hydrocephalus
Canadian Journal of Neurological Sciences
Medicine
Neurology
Genetic Study of Three Closely Linked X Chromosome STR Markers in an Argentinian Population | Journal of Forensic Investigation
Journal of Forensic Investigation
