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1,337 results
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Page 1
GPC3 mutations in seven patients with Simpson-Golabi-Behmel syndrome.
Sakazume S, Okamoto N, Yamamoto T, Kurosawa K, Numabe H, Ohashi Y, Kako Y, Nagai T, Ohashi H. Sakazume S, et al. Among authors: ohashi y, ohashi h. Am J Med Genet A. 2007 Aug 1;143A(15):1703-7. doi: 10.1002/ajmg.a.31822. Am J Med Genet A. 2007. PMID: 17603795
[Chromosome 22].
Ohashi H. Ohashi H. Ryoikibetsu Shokogun Shirizu. 2001;(33):440-1. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462505 Review. Japanese. No abstract available.
[Chromosome 17].
Ohashi H. Ohashi H. Ryoikibetsu Shokogun Shirizu. 2001;(33):428-30. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462500 Review. Japanese. No abstract available.
[Chromosome 20].
Ohashi H. Ohashi H. Ryoikibetsu Shokogun Shirizu. 2001;(33):435-6. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462503 Review. Japanese. No abstract available.
[Asplenia syndrome (Ivemark syndrome)].
Ohashi H, Yamaguchi M. Ohashi H, et al. Ryoikibetsu Shokogun Shirizu. 1996;(15):334-6. Ryoikibetsu Shokogun Shirizu. 1996. PMID: 9048035 Review. Japanese. No abstract available.
[Nail-patella syndrome].
Ohashi H. Ohashi H. Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):215-7. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11057202 Review. Japanese. No abstract available.
[Femoral hypoplasia-unusual facies syndrome].
Ohashi H. Ohashi H. Ryoikibetsu Shokogun Shirizu. 2001;(33):670-1. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462625 Review. Japanese. No abstract available.
1,337 results