Genetics

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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

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