S C Saitta - JoVE Visualize

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Advances in Pediatrics|August 2, 2001

The 22q11.2 deletion syndromeB S Emanuel, D McDonald-McGinn, S C Saitta, et al.

Human Molecular Genetics|March 4, 2000

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysisT H Shaikh, H Kurahashi, S C Saitta, et al.

Molecular Syndromology|July 26, 2013

More Clinical Overlap between 22q11.2 Deletion Syndrome and CHARGE Syndrome than Often AnticipatedN Corsten-Janssen, S C Saitta, L H Hoefsloot, et al.

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Showing results (1-10 of 3) with videos related to

Sort By:

Pageof 1

Advances in Pediatrics|August 2, 2001

The 22q11.2 deletion syndromeB S Emanuel, D McDonald-McGinn, S C Saitta, et al.

Human Molecular Genetics|March 4, 2000

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysisT H Shaikh, H Kurahashi, S C Saitta, et al.

Molecular Syndromology|July 26, 2013

More Clinical Overlap between 22q11.2 Deletion Syndrome and CHARGE Syndrome than Often AnticipatedN Corsten-Janssen, S C Saitta, L H Hoefsloot, et al.

Pageof 1