Matches in Nanopublications for { ?s ?p "[Although our data provide no overall support for association of CDH2 rare variants in these disorders considered as single entities, the clinical features and severity of probands carrying the uncommon non-synonymous variants suggest that CDH2, along with other cadherin and cell adhesion genes, is an interesting gene to pursue as a plausible contributor to OCD, TD and related disorders with repetitive behaviors, including autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Although our data provide no overall support for association of CDH2 rare variants in these disorders considered as single entities, the clinical features and severity of probands carrying the uncommon non-synonymous variants suggest that CDH2, along with other cadherin and cell adhesion genes, is an interesting gene to pursue as a plausible contributor to OCD, TD and related disorders with repetitive behaviors, including autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_assertion description "[Although our data provide no overall support for association of CDH2 rare variants in these disorders considered as single entities, the clinical features and severity of probands carrying the uncommon non-synonymous variants suggest that CDH2, along with other cadherin and cell adhesion genes, is an interesting gene to pursue as a plausible contributor to OCD, TD and related disorders with repetitive behaviors, including autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_provenance.
- NP299930.RAWQshDAMzE2EHPdY2g9gqjl2htTD7faaapsH1Z4gLBcY130_assertion description "[Although our data provide no overall support for association of CDH2 rare variants in these disorders considered as single entities, the clinical features and severity of probands carrying the uncommon non-synonymous variants suggest that CDH2, along with other cadherin and cell adhesion genes, is an interesting gene to pursue as a plausible contributor to OCD, TD and related disorders with repetitive behaviors, including autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP299930.RAWQshDAMzE2EHPdY2g9gqjl2htTD7faaapsH1Z4gLBcY130_provenance.
- NP1044174.RAX9QSm7c8sNYrNu4XiRzttRcbJ3_6VWcSbfPr6ug3eug130_assertion description "[Although our data provide no overall support for association of CDH2 rare variants in these disorders considered as single entities, the clinical features and severity of probands carrying the uncommon non-synonymous variants suggest that CDH2, along with other cadherin and cell adhesion genes, is an interesting gene to pursue as a plausible contributor to OCD, TD and related disorders with repetitive behaviors, including autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1044174.RAX9QSm7c8sNYrNu4XiRzttRcbJ3_6VWcSbfPr6ug3eug130_provenance.
- NP299906.RACpndzIdEkjb8qWVkBvP_8Y6IsF9Eo6Go1hDFQo9jgKU130_assertion description "[Although our data provide no overall support for association of CDH2 rare variants in these disorders considered as single entities, the clinical features and severity of probands carrying the uncommon non-synonymous variants suggest that CDH2, along with other cadherin and cell adhesion genes, is an interesting gene to pursue as a plausible contributor to OCD, TD and related disorders with repetitive behaviors, including autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP299906.RACpndzIdEkjb8qWVkBvP_8Y6IsF9Eo6Go1hDFQo9jgKU130_provenance.
- NP1044172.RAFwhHVvELfutL5YJivsshvxlTHBZ_iwiNvrcA0wzjufY130_assertion description "[Although our data provide no overall support for association of CDH2 rare variants in these disorders considered as single entities, the clinical features and severity of probands carrying the uncommon non-synonymous variants suggest that CDH2, along with other cadherin and cell adhesion genes, is an interesting gene to pursue as a plausible contributor to OCD, TD and related disorders with repetitive behaviors, including autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1044172.RAFwhHVvELfutL5YJivsshvxlTHBZ_iwiNvrcA0wzjufY130_provenance.