Clinical management of patients with ASXL1 mutations and Bohring–Opitz syndrome, emphasizing the need for Wilms tumor surveillance
B Russell, JJ Johnston, LG Biesecker… - American Journal of …, 2015 - Wiley Online Library
Bohring–Opitz syndrome is a rare genetic condition characterized by distinctive facial
features, variable microcephaly, hypertrichosis, nevus flammeus, severe myopia, unusual …
features, variable microcephaly, hypertrichosis, nevus flammeus, severe myopia, unusual …
[HTML][HTML] Clinical Management of Patients with ASXL1 Mutations and Bohring-Opitz Syndrome, Emphasizing the Need for Wilms Tumor Surveillance
B Russell, JJ Johnston, LG Biesecker… - American journal of …, 2015 - ncbi.nlm.nih.gov
Bohring-Opitz syndrome is a rare genetic condition characterized by distinctive facial
features, variable microcephaly, hypertrichosis, nevus flammeus, severe myopia, unusual …
features, variable microcephaly, hypertrichosis, nevus flammeus, severe myopia, unusual …
Clinical management of patients with ASXL1 mutations and Bohring–Opitz syndrome, emphasizing the need for Wilms tumor surveillance
B Russell, JJ Johnston, LG Biesecker… - American Journal of …, 2015 - cir.nii.ac.jp
抄録< jats: sec>< jats: label/>< jats: p> Bohring–Opitz syndrome is a rare genetic condition
characterized by distinctive facial features, variable microcephaly, hypertrichosis, nevus …
characterized by distinctive facial features, variable microcephaly, hypertrichosis, nevus …
Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance.
B Russell, JJ Johnston, LG Biesecker… - American Journal of …, 2015 - europepmc.org
Bohring-Opitz syndrome is a rare genetic condition characterized by distinctive facial
features, variable microcephaly, hypertrichosis, nevus flammeus, severe myopia, unusual …
features, variable microcephaly, hypertrichosis, nevus flammeus, severe myopia, unusual …
[PDF][PDF] Clinical Management of Patients with ASXL1 Mutations and Bohring–Opitz Syndrome, Emphasizing the Need for Wilms Tumor Surveillance
B Russell, JJ Johnston, LG Biesecker, N Kramer… - 2015 - researchgate.net
Bohring–Opitz syndrome (BOS), previously reported as Oberklaid–Danks syndrome, is a
rare genetic condition that was initially distinguished from Opitz Trigonocephaly C syndrome …
rare genetic condition that was initially distinguished from Opitz Trigonocephaly C syndrome …
[PDF][PDF] Clinical Management of Patients with ASXL1 Mutations and Bohring–Opitz Syndrome, Emphasizing the Need for Wilms Tumor Surveillance
B Russell, JJ Johnston, LG Biesecker, N Kramer… - 2015 - academia.edu
Bohring–Opitz syndrome (BOS), previously reported as Oberklaid–Danks syndrome, is a
rare genetic condition that was initially distinguished from Opitz Trigonocephaly C syndrome …
rare genetic condition that was initially distinguished from Opitz Trigonocephaly C syndrome …
Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance
B Russell, JJ Johnston, LG Biesecker… - American Journal of …, 2015 - pure.johnshopkins.edu
Bohring-Opitz syndrome is a rare genetic condition characterized by distinctive facial
features, variable microcephaly, hypertrichosis, nevus flammeus, severe myopia, unusual …
features, variable microcephaly, hypertrichosis, nevus flammeus, severe myopia, unusual …
Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance
B Russell, JJ Johnston… - … journal of medical …, 2015 - pubmed.ncbi.nlm.nih.gov
Bohring-Opitz syndrome is a rare genetic condition characterized by distinctive facial
features, variable microcephaly, hypertrichosis, nevus flammeus, severe myopia, unusual …
features, variable microcephaly, hypertrichosis, nevus flammeus, severe myopia, unusual …
Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance.
B Russell, JJ Johnston, LG Biesecker… - American Journal of …, 2015 - europepmc.org
Bohring-Opitz syndrome is a rare genetic condition characterized by distinctive facial
features, variable microcephaly, hypertrichosis, nevus flammeus, severe myopia, unusual …
features, variable microcephaly, hypertrichosis, nevus flammeus, severe myopia, unusual …