Rubinstein-Taybi syndrome 2 with cerebellar abnormality and neural
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Congenital basis of posterior fossa anomalies - Claudia Cotes
Expanding the phenotype associated to KMT2A variants: overlapping
Rubinstein–Taybi syndrome: New neuroradiological and
Frontiers Olfactory Malformations in Mendelian Disorders of the
Congenital Abnormalities of the Brain
Congenital basis of posterior fossa anomalies. - Abstract - Europe PMC
Rubinstein-Taybi Syndrome 2 disease: Malacards - Research Articles
Pediatrics Neupsy Key
Rubinstein-Taybi syndrome: MedlinePlus Genetics
Frontiers An Early Diagnostic Clue for COL18A1- and LAMA1
a,b: Patient A at 3 weeks; c,d: Patient B at 6 weeks, note the
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of
PDF) Rubinstein–Taybi syndrome 2 with cerebellar abnormality and
Rubinstein-Taybi syndrome with scoliosis treated with single-stage
Skeletal Dysplasias - Endotext - NCBI Bookshelf
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