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One or more keywords matched the following items that are connected to
Lyons, Michael
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Academic Article
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Genome-wide linkage analysis of heroin dependence in Han Chinese: results from wave one of a multi-stage study.
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Academic Article
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Ordered subsets linkage analysis of antisocial behavior in substance use disorder among participants in the Collaborative Study on the Genetics of Alcoholism.
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Academic Article
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FG syndrome, an X-linked multiple congenital anomaly syndrome: the clinical phenotype and an algorithm for diagnostic testing.
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Academic Article
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Genome-wide linkage analysis of heroin dependence in Han Chinese: results from Wave Two of a multi-stage study.
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Academic Article
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Autism in two females with duplications involving Xp11.22-p11.23.
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Academic Article
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Chromosome 22q11.2 deletion syndrome in African-American patients: a diagnostic challenge.
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Academic Article
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Unbalanced translocation involving partial trisomy 9p and partial monosomy yq with neurodevelopmental delays.
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Academic Article
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Clinical utility of the X-chromosome array.
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Concept
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Chromosomes, Human, Y
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Concept
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Chromosomes, Human, Pair 16
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Concept
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Chromosomes, Human, Pair 17
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Concept
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Chromosomes, Human
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Concept
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Chromosomes, Human, Pair 4
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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 6
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Concept
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Chromosomes, Human, Pair 9
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Concept
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Chromosomes, Human, Pair 22
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Concept
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Chromosomes, Human, X
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Concept
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Chromosomes, Human, Pair 3
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Academic Article
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Acquired microcephaly in blepharophimosis-ptosis-epicanthus inversus syndrome because of an interstitial 3q22.3q23 deletion.
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Academic Article
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Neurodevelopmental delays and macrocephaly in 17p13.1 microduplication syndrome.
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Academic Article
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Deletion of 16q24.1 supports a role for the ATP2C2 gene in specific language impairment.
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Academic Article
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Microdeletions on 6p22.3 are associated with mesomelic dysplasia Savarirayan type.
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