Preferential Paternal Origin of Microdeletions Caused by Prezygotic Chromosome or Chromatid Rearrangements in Sotos Syndrome
The American Journal of Human Genetics2003Vol. 72(5), pp. 1331–1337
Citations Over TimeTop 10% of 2003 papers
Noriko Miyake, Naohiro Kurotaki, Hirobumi Sugawara, Osamu Shimokawa, Naoki Harada, Tatsuro Kondoh, Masato Tsukahara, Satoshi Ishikiriyama, Tohru Sonoda, Yoko Miyoshi, Satoru Sakazume, Yoshimitsu Fukushima, Hirofumi Ohashi, Toshiro Nagai, Hiroshi Kawame, Kenji Kurosawa, Mayumi Touyama, Takashi Shiihara, Nobuhiko Okamoto, Junji Nishimoto, Ko‐ichiro Yoshiura, Tohru Ohta, Tatsuya Kishino, Norio Niikawa, Naomichi Matsumoto
Related Papers
- → Haploinsufficiency of NSD1 causes Sotos syndrome(2002)655 cited
- → NSD1 mutations in Sotos syndrome(2005)51 cited
- → Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephaly(2007)28 cited
- → Sotos syndrome in two children from India(2020)3 cited
- → Diagnosing Sotos Syndrome in the Setting of Global Developmental Delay and Macrocephaly(2006)6 cited