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LALANI, SEEMA
One or more keywords matched the following items that are connected to
LALANI, SEEMA
Item Type
Name
Concept
Dwarfism
Academic Article
Heterozygous deletion of exons 18 and 19 of IGF1R in an individual with short stature.
Academic Article
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
Academic Article
CRIPT exonic deletion and a novel missense mutation in a female with short stature, dysmorphic features, microcephaly, and pigmentary abnormalities.
Academic Article
Clinical Characterization of Patients With Autosomal Dominant Short Stature due to Aggrecan Mutations.
Search Criteria
Dwarfism