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RS

Robert Saul

Medical Genetics / Clinical Genetics (M.D.)

Credentials: ·

History

Pediatrics

Research

22q13 deletion syndrome
American Journal of Medical Genetics · 2001 · 209 citations
Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations
European Journal of Human Genetics · 2014 · 73 citations
Constitutional and mosaic large NF1 gene deletions in neurofibromatosis type 1
Journal of Medical Genetics · 1998 · 72 citations

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