[HTML][HTML] De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome …
Abstract Background Wiedemann-Steiner Syndrome (WSS) is characterized by short stature,
a variety of dysmorphic facial and skeletal features, characteristic hypertrichosis cubiti …
a variety of dysmorphic facial and skeletal features, characteristic hypertrichosis cubiti …
De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing
SP Strom, R Lozano, H Lee, N Dorrani… - BMC Medical …, 2014 - escholarship.org
BackgroundWiedemann-Steiner Syndrome (WSS) is characterized by short stature, a variety
of dysmorphic facial and skeletal features, characteristic hypertrichosis cubiti (excessive hair …
of dysmorphic facial and skeletal features, characteristic hypertrichosis cubiti (excessive hair …
De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing.
SP Strom, R Lozano, H Lee, N Dorrani… - BMC Medical …, 2014 - search.ebscohost.com
Abstract Background Wiedemann-Steiner Syndrome (WSS) is characterized by short stature,
a variety of dysmorphic facial and skeletal features, characteristic hypertrichosis cubiti …
a variety of dysmorphic facial and skeletal features, characteristic hypertrichosis cubiti …
[HTML][HTML] De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome …
SP Strom, R Lozano, H Lee, N Dorrani… - BMC Medical …, 2014 - ncbi.nlm.nih.gov
Background Wiedemann-Steiner Syndrome (WSS) is characterized by short stature, a
variety of dysmorphic facial and skeletal features, characteristic hypertrichosis cubiti …
variety of dysmorphic facial and skeletal features, characteristic hypertrichosis cubiti …
[HTML][HTML] De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome …
SP Strom, R Lozano, H Lee… - BMC Medical …, 2014 - bmcmedgenet.biomedcentral.com
Wiedemann-Steiner Syndrome (WSS) is characterized by short stature, a variety of
dysmorphic facial and skeletal features, characteristic hypertrichosis cubiti (excessive hair …
dysmorphic facial and skeletal features, characteristic hypertrichosis cubiti (excessive hair …
[PDF][PDF] De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing
SP Strom, R Lozano, H Lee, N Dorrani, J Mann… - 2014 - Citeseer
Abstract Background: Wiedemann-Steiner Syndrome (WSS) is characterized by short
stature, a variety of dysmorphic facial and skeletal features, characteristic hypertrichosis …
stature, a variety of dysmorphic facial and skeletal features, characteristic hypertrichosis …
[PDF][PDF] De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing
SP Strom, R Lozano, H Lee, N Dorrani, J Mann… - 2014 - cyberleninka.org
Abstract Background: Wiedemann-Steiner Syndrome (WSS) is characterized by short
stature, a variety of dysmorphic facial and skeletal features, characteristic hypertrichosis …
stature, a variety of dysmorphic facial and skeletal features, characteristic hypertrichosis …
[PDF][PDF] De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing
SP Strom, R Lozano, H Lee, N Dorrani, J Mann… - 2014 - researchgate.net
Abstract Background: Wiedemann-Steiner Syndrome (WSS) is characterized by short
stature, a variety of dysmorphic facial and skeletal features, characteristic hypertrichosis …
stature, a variety of dysmorphic facial and skeletal features, characteristic hypertrichosis …
[引用][C] De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing
SP Strom, R Lozano, H Lee, N Dorrani, J Mann… - BMC Medical …, 2014 - cir.nii.ac.jp
De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in
two unrelated individuals identified by clinical exome sequencing | CiNii Research CiNii 国立 …
two unrelated individuals identified by clinical exome sequencing | CiNii Research CiNii 国立 …
De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing
SP Strom, R Lozano, H Lee, N Dorrani… - BMC medical …, 2014 - pubmed.ncbi.nlm.nih.gov
Background Wiedemann-Steiner Syndrome (WSS) is characterized by short stature, a
variety of dysmorphic facial and skeletal features, characteristic hypertrichosis cubiti …
variety of dysmorphic facial and skeletal features, characteristic hypertrichosis cubiti …