Genetics 1968, Congenital Dysplasia of the Hip in the Navajo Infant 1970, Cleft Palate , cleft lip, cleft uvula in Navajo Indians 1977, Astigmatism in Zuni & Navajo 1977, Atypical and Fluoride-Resistant Cholinesterase Genes-Absent in a Native American Indian Population 1981, Retinitis Pigmentosa in the Navajo 1990, Neuropathy in Navajo children-clinical and epidemiologic features 1991, Severe Combined Immunodeficiency among the Navajo. I. Characterization of Phenotypes, Epidemiology, and Population Genetics 1992, Lynch Syndrom II in a Navajo Family-A revisit 1993, Familial sensory autonomic neuropathy with arthropathy in Navajo children 1994, Metachromatic Leukodystrophy in the Navajo Indian Population- A Splice Site Mutation in Intron 4 of the Arylsulfatase A Gene 1994, Mutation of an mutL homologue in a Navajo family with hereditary nonpolyposis colorectal cancer 1999, A cluster of microvillous inclusion disease in the Navajo population 1999, Liver disease in Navajo neuropathy 2000, Assessment of serum-mediated neurotoxicity in navajo neuropathy 2001, Metachromatic leukodystrophy in the Navajo- fallout of the American-Indian wars of the nineteenth century 2001, Navajo Neurohepatopathy- A Mitochondrial DNA Depletion Syndrome 2002, Navajo Neuropathy- Relation to MDR3 mRNA Deficiency 2002, Prenatal diagnosis and carrier detection for Athabascan severe combined immunodeficiency disease 2003, A 122.5-Kilobase Deletion of the P Gene Underlies the High Prevalence of Oculocutaneous Albinism Type 2 in the Navajo Population 2003, Absence of RECQL4 mutations in poikiloderma with neutropenia in Navajo and non-Navajo patients 2003, Athabascan Brainstem Dysgenesis Syndrome 2006, Navajo neuropathy is caused by a mutations in the mpv17 gene 2007, Oro-facial-digital syndrome IX with severe microcephaly- a new variant in a genetically isolated population 2008, Navajo microvillous inclusion disease is due to a mutation in MYO5B 2009, Autosomal recessive diseases among the Athabaskans of the southwestern United States- recent advances and implications for the future 2010, MPV17-associated hepatocerebral mitochondrial DNA depletion syndrome- New patients and novel mutations 2010, Orthopaedic Manifestations of Navajo Familial Neurogenic Arthropathy 2011, Detection of G3P-3 and G3P-9 Rotavirus Strains in American Indian Children With Evidence of Gene Reassortment Between Human and Animal Rotaviruses