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Publications by Abbe N. Vallejo
Mutations in the Human SC4MOL Gene Encoding a Methyl Sterol Oxidase Cause Psoriasiform Dermatitis, Microcephaly, and Developmental Delay
Journal of Clinical Investigation
Medicine
Comparable Genital Tract Infection, Pathology, and Immunity in Rhesus Macaques Inoculated With Wild-Type or Plasmid-Deficient Chlamydia Trachomatis Serovar D
Infection and Immunity
Parasitology
Infectious Diseases
Immunology
Microbiology
Related publications
Human Mutations in NDE1 Cause Extreme Microcephaly With Lissencephaly
American Journal of Human Genetics
Genetics
The Role of Sterol-C4-Methyl Oxidase in Epidermal Biology
Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids
Cell Biology
Molecular Biology
Bi-Allelic ADPRHL2 Mutations Cause Neurodegeneration With Developmental Delay, Ataxia, and Axonal Neuropathy
American Journal of Human Genetics
Genetics
Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart Defects
American Journal of Human Genetics
Genetics
Mutations in the Human TBX4 Gene Cause Small Patella Syndrome
American Journal of Human Genetics
Genetics
Joubert Syndrome: A Rare Cause for Developmental Delay
Journal of Medical Science And clinical Research
Mutations in KEOPS-complex Genes Cause Nephrotic Syndrome With Primary Microcephaly
Nature Genetics
Genetics
Psoriasiform Lichenoid Dermatitis in the Springer Spaniel
Veterinary Pathology
Veterinary
The Prevalence of Mutations in the Gene Encoding Filaggrin in the Population of Polish Patients With Atopic Dermatitis
Postepy Dermatologii I Alergologii
Dermatology
Allergy
Immunology
