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Index « Auteurs » - entrée « Tsutomu Ogata »
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List of bibliographic references indexed by Tsutomu Ogata

Number of relevant bibliographic references: 9.
Ident.Authors (with country if any)Title
001515 (2016) Antonio Marchini ; Tsutomu Ogata ; Gudrun A. RappoldA Track Record on SHOX: From Basic Research to Complex Models and Therapy
005D18 (2010) Harunosuke Kato [Japon] ; Rie Yoshida [Japon] ; Katsuhiko Tsukamoto [Japon] ; Hirotaka Suga [Japon] ; Hitomi Eto [Japon] ; Takuya Higashino [Japon] ; Jun Araki [Japon] ; Tsutomu Ogata [Japon] ; Kotaro Yoshimura [Japon]Familial cases of atypical clinical features genetically diagnosed as LEOPARD syndrome (multiple lentigines syndrome)
008C82 (2004) Rie Yoshida [Japon] ; Masafumi Miyata [Japon] ; Toshiro Nagai [Japon] ; Toshio Yamazaki [Japon] ; Tsutomu Ogata [Japon]A 3‐bp deletion mutation of PTPN11 in an infant with severe Noonan syndrome including hydrops fetalis and juvenile myelomonocytic leukemia
008E51 (2003) Tsutomu Ogata [Japon] ; Seiji Sato ; Yukihiro Hasegawa ; Kenjiro KosakiLymphstasis in a boy with Noonan syndrome: implication for the development of skeletal features.
009373 (2002) Tsutomu Ogata [Japon]SHOX haploinsufficiency and its modifying factors.
009873 (2002) Tsutomu Ogata [Japon] ; Koji Muroya [Japon] ; Goro Sasaki [Japon] ; Gen Nishimura [Japon] ; Hiroshi Kitoh [Japon] ; Tadashi Hattori [Japon]SHOX nullizygosity and haploinsufficiency in a japanese family : Implication for the development of Turner skeletal features
00A031 (2001) Catherine A. Boucher ; Carole A. Sargent ; Tsutomu Ogata ; Nabeel A. AffaraBreakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location [Original article] [Original article]
00C117 (1996) Tomonobu Hasegawa [Japon] ; Tsutomu Ogata [Japon] ; Yukihiro Hasegawa [Japon] ; Masataka Honda [Japon] ; Toshiro Nagai [Japon] ; Yoshimitsu Fukushima [Japon] ; Yutaka Nakahori [Japon] ; Nobutake Matsuo [Japon]Coarctation of the aorta and renal hypoplasia in a boy with Turner/Noonan surface anomalies and a 46,XY karyotype: A clinical model for the possible impairment of a putative lymphogenic gene(s) for Turner somatic stigmata
00C484 (1995) Tsutomu Ogata [Japon] ; Nobutake Matsuo [Japon]Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features

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