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One or more keywords matched the following items that are connected to Strauss, Kevin
Item TypeName
Concept Chromosomes, Human, Pair 7
Concept Chromosomes, Human, Pair 19
Concept Chromosomes, Human, Pair 3
Concept Chromosomes, Human, Pair 20
Concept Chromosomes, Human, Pair 5
Concept Chromosome Mapping
Concept Chromosomes, Human, Pair 2
Academic Article Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function.
Academic Article Type I glutaric aciduria, part 1: natural history of 77 patients.
Academic Article Genome-wide SNP arrays as a diagnostic tool: clinical description, genetic mapping, and molecular characterization of Salla disease in an Old Order Mennonite population.
Academic Article Monoallelic BMP2 Variants Predicted to Result in Haploinsufficiency Cause Craniofacial, Skeletal, and Cardiac Features Overlapping Those of 20p12 Deletions.
Academic Article Spinal muscular atrophy within Amish and Mennonite populations: Ancestral haplotypes and natural history.
Academic Article Polyhydramnios, megalencephaly and symptomatic epilepsy caused by a homozygous 7-kilobase deletion in LYK5.
Academic Article Genetics, medicine, and the Plain people.
Academic Article Human ITCH E3 ubiquitin ligase deficiency causes syndromic multisystem autoimmune disease.
Academic Article A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome.
Academic Article Genetic mapping of glutaric aciduria, type 3, to chromosome 7 and identification of mutations in c7orf10.
Academic Article Genetic mapping and exome sequencing identify variants associated with five novel diseases.
Academic Article A homozygous missense mutation in HERC2 associated with global developmental delay and autism spectrum disorder.
Search Criteria
  • Chromosomes Human Pair 8