Condition: Delayed bone age
rs1561873941
in
CUL7
gene and
Delayed bone age
PMID 30980518
2019 Further expanding the mutational spectrum and investigation of genotype-phenotype correlation in 3M syndrome.
rs1561875767
in
CUL7;KLC4
gene and
Delayed bone age
PMID 30980518
2019 Further expanding the mutational spectrum and investigation of genotype-phenotype correlation in 3M syndrome.
rs864309486
in
GMNN
gene and
Delayed bone age
PMID 26637980
2015 De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
rs1559155800
in
OBSL1
gene and
Delayed bone age
PMID 30980518
2019 Further expanding the mutational spectrum and investigation of genotype-phenotype correlation in 3M syndrome.