Pages that link to "Q87824661"
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The following pages link to Paulien A Terhal (Q87824661):
Displaying 5 items.
- Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosis (Q35969087) (← links)
- Two novel cases expanding the phenotype of SETD2-related overgrowth syndrome. (Q52571935) (← links)
- Further delineation of the GDF6 related multiple synostoses syndrome. (Q52790573) (← links)
- Further delineation of an entity caused by CREBBP and EP300 mutations but not resembling Rubinstein-Taybi syndrome. (Q54270426) (← links)
- Meier-Gorlin syndrome: Growth and secondary sexual development of a microcephalic primordial dwarfism disorder (Q57199245) (← links)