A patient with constitutional ring 1 chromosome characterized by SNP array CGH

Por Saliganan, Sheila, Lee, Joanna, Wei, Sainan
Publicado no Clin Case Rep (2016)

Seizures as the first manifestation of chromosome 22q11.2 deletion syndrome in a 40-year old man: a case report

Por Tonelli Adriano R, Kosuri Kalyan, Wei Sainan, Chick Davoren
Publicado em 2007-12-01

Seizures as the first manifestation of chromosome 22q11.2 deletion syndrome in a 40-year old man: a case report

Por Tonelli, Adriano R, Kosuri, Kalyan, Wei, Sainan, Chick, Davoren
Publicado em 2007

Frontofacionasal Dysplasia in a Newborn with a De Novo Duplication of 7p15.2-p15.1

Por Mansour, Tamer, Wei, Sainan, Netzloff, Michael, Mohamed, Tarek, Schutte, Brian, Omar, Said A.
Publicado no AJP Rep (2015)

Isodicentric Y Mosaicism Involving a 46, XX Cell Line: Implications for Management

Por Hipp, Lauren E., Mohnach, Lauren, Wei, Sainan, Thomas, Inas H., Elhassan, Maha, Sandberg, David E., Quint, Elisabeth H., Keegan, Catherine E.
Publicado no Am J Med Genet A (2015)