Beemer

释义

[人名] 比默；[地名] [美国] 比默；

Functional Outcome in Osteogenesis Imperfecta: Disability Profiles Using the PEDI
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans.
The 22q11.2 Deletion in Children
Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counselling.
Cerebral gigantism (Sotos syndrome). Compiled data of 22 cases. Analysis of clinical features, growth and plasma somatomedin
Annual migrations, diving behavior, and thermal biology of Atlantic bluefin tuna, Thunnus thynnus , on their Gulf of Mexico breeding...
Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies:...
The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms.
Characterisation of deletions of the ZFHX1B region and genotype-phenotype analysis in Mowat-Wilson syndrome.
Accessing financial accounts with 3D bar code