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One or more keywords matched the following items that are connected to
Strauss, Kevin
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Concept
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Chromosomes, Human, Pair 7
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Concept
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Chromosomes, Human, Pair 19
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Concept
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Chromosomes, Human, Pair 3
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Concept
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Chromosomes, Human, Pair 20
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Concept
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Chromosomes, Human, Pair 5
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Concept
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Chromosomes, Human, Pair 2
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Academic Article
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Type I glutaric aciduria, part 1: natural history of 77 patients.
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Academic Article
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Monoallelic BMP2 Variants Predicted to Result in Haploinsufficiency Cause Craniofacial, Skeletal, and Cardiac Features Overlapping Those of 20p12 Deletions.
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Academic Article
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Spinal muscular atrophy within Amish and Mennonite populations: Ancestral haplotypes and natural history.
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Academic Article
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Human ITCH E3 ubiquitin ligase deficiency causes syndromic multisystem autoimmune disease.
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Academic Article
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A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome.
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Academic Article
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Genetic mapping of glutaric aciduria, type 3, to chromosome 7 and identification of mutations in c7orf10.
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