Rubinstein-Taybi syndrome: MedlinePlus Genetics
Por um escritor misterioso
Descrição
Rubinstein-Taybi syndrome is a condition characterized by short stature, moderate to severe intellectual disability, distinctive facial features, and broad thumbs and first toes . Explore symptoms, inheritance, genetics of this condition.
Otopalatodigital Syndrome, Type I disease: Malacards - Research
Rubinstein–Taybi syndrome European Journal of Human Genetics
The behavioral phenotype of Rubinstein–Taybi syndrome: A scoping
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With
How Are Changes in the Chromosome 16 Related to Health Conditions
Floating-Harbor syndrome: MedlinePlus Genetics
Chromosome 16: MedlinePlus Genetics
Pediatric on Squares on X: Rubinstein Taybi Syndrome #Pediatric
Floating-Harbor syndrome: MedlinePlus Genetics
What is EP300 Gene Rubinstein-Taybi syndrome NGS Genetic DNA Test ?
de
por adulto (o preço varia de acordo com o tamanho do grupo)
