[HTML][HTML] Wiedemann–Steiner Syndrome: Case Report and Review of Literature

H Yu, G Zhang, S Yu, W Wu - Children, 2022 - mdpi.com
Wiedemann–Steiner syndrome (WDSTS) is an autosomal dominant disorder with a broad
and variable phenotypic spectrum characterized by intellectual disability, prenatal and …

[HTML][HTML] Wiedemann–Steiner Syndrome: Case Report and Review of Literature

H Yu, G Zhang, S Yu, W Wu - Children, 2022 - ncbi.nlm.nih.gov
Wiedemann–Steiner syndrome (WDSTS) is an autosomal dominant disorder with a broad
and variable phenotypic spectrum characterized by intellectual disability, prenatal and …

Wiedemann–Steiner Syndrome: Case Report and Review of Literature.

H Yu, G Zhang, S Yu, W Wu - Children, 2022 - search.ebscohost.com
Wiedemann–Steiner syndrome (WDSTS) is an autosomal dominant disorder with a broad
and variable phenotypic spectrum characterized by intellectual disability, prenatal and …

Wiedemann-Steiner Syndrome: Case Report and Review of Literature.

H Yu, G Zhang, S Yu, W Wu - Children (Basel, Switzerland), 2022 - europepmc.org
Wiedemann-Steiner syndrome (WDSTS) is an autosomal dominant disorder with a broad
and variable phenotypic spectrum characterized by intellectual disability, prenatal and …

Wiedemann-Steiner Syndrome: Case Report and Review of Literature

H Yu, G Zhang, S Yu, W Wu - Children (Basel, Switzerland …, 2022 - pubmed.ncbi.nlm.nih.gov
Wiedemann-Steiner syndrome (WDSTS) is an autosomal dominant disorder with a broad
and variable phenotypic spectrum characterized by intellectual disability, prenatal and …

Wiedemann–Steiner Syndrome: Case Report and Review of Literature

H Yu, G Zhang, S Yu, W Wu - Children, 2022 - search.proquest.com
Wiedemann–Steiner syndrome (WDSTS) is an autosomal dominant disorder with a broad
and variable phenotypic spectrum characterized by intellectual disability, prenatal and …

Wiedemann–Steiner Syndrome: Case Report and Review of Literature

H Yu, G Zhang, S Yu, W Wu - Children, 2022 - europepmc.org
Wiedemann–Steiner syndrome (WDSTS) is an autosomal dominant disorder with a broad
and variable phenotypic spectrum characterized by intellectual disability, prenatal and …