Channels :: FRELIP Discovery

Author: Simonic, Ingrid

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The search for tourette syndrome genes : a conceptual and experimental approach

Similar Items: The search for tourette syndrome genes : a conceptual and experimental approach

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The influence of therapeutic horse riding on neuropsychological outcomes in children with Tourette Syndrome
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Molecular and functional characterisation of Long QT Syndrome causing genes
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Ethical aspects of genetic information about hereditary cancer syndromes
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A molecular investigation of Waardenburg syndrome in Southern Africa
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The Outcomes of infants with Edward Syndrome and Patau Syndrome in a resource restricted environment
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Characterisation of novel TAC3 and TACR3 gene variants and polymorphisms in patients with pre-eclampsia
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A genetic study of long QT syndrome in two South African families
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Molecular analysis of GJB2 (connexin 26) and GJB6 (connexin 30) gene mutations in non-syndromic hereditary deafness in South Africa
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A Case Report of Shwachman‐Diamond Syndrome Caused by Heterozygous Variants in the EFL1 Gene and Literature Review
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Kufor–Rakeb Syndrome in a Guatemalan Patient With an ATP13A2 Gene Pathogenic Variant: A Case Report
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A Case of Malan Syndrome With Pulmonary Artery Dilatation due to a Novel Frameshift Variant in Exon 2 of the NFIX Gene
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Long QT syndrome : the identification and verification of putative KCNE2-interacting proteins
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Analysis of genetic variants in the 5’ regulatory region of the ALAS1 gene in South African patients with Variegate Porphyria (VP)
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An investigation of the clinical profile and extent of Long QT Syndrome (LQTS) associated with the KCNQ1-A341V mutation in South Africa and with the KCNH2-A1116V mutation in an Italian family and the role that autonomic nervous system (ANS) activity and genetics play in clinical variability
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Transformation of Nicotiana tabacum cv. Samsun with melanin and indigo genes
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Genetic Analysis of Pitt–Hopkins Syndrome Caused by a Novel Splicing Variant (c.1146+3A>T) in the TCF4 Gene
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Mutation screening of pre-eclampsia candidate genes, LEP (ob) and LEPR (obR)
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Tagging and mapping of prominent structural genes on chromosome arm 7DL of common wheat
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Genetic association analysis of polymorphisms in four cytochrome P450 genes, the MDR1 gene and treatment-outcome in Xhosa schizophrenia patients
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Molecular characterisation of the gene, LGALS13, and its putative involvement in pre-eclampsia
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A c.89G>C p.(Gly30Ala) Variant in the DHCR7 Gene as a Cause of a Mild Phenotype in the Smith‐Lemli‐Opitz Syndrome
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A characterisation of genes involved in apoptosis resistance
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A candidate and novel gene search to identify the PFHBII-causative gene
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A Case of Pallister–Killian Syndrome in a Newborn