Sugio Y - Search Results

1

No evidence of PEG1/MEST gene mutations in Silver-Russell syndrome patients.

Kobayashi S, Uemura H, Kohda T, Nagai T, Chinen Y, Naritomi K, Kinoshita EI, Ohashi H, Imaizumi K, Tsukahara M, Sugio Y, Tonoki H, Kishino T, Tanaka T, Yamada M, Tsutsumi O, Niikawa N, Kaneko-Ishino T, Ishino F. Kobayashi S, et al. Among authors: sugio y. Am J Med Genet. 2001 Dec 1;104(3):225-31. Am J Med Genet. 2001. PMID: 11754049

2

Median nodule of the upper lip: an autosomal dominant trait.

Tsukahara M, Fernandez I, Sugio Y, Shiota K. Tsukahara M, et al. Among authors: sugio y. Am J Med Genet. 1994 May 15;51(1):13-5. doi: 10.1002/ajmg.1320510104. Am J Med Genet. 1994. PMID: 8030663

3

Translocation t(X;21)(q13.3; p11.1) in a girl with Menkes disease.

Sugio Y, Sugio Y, Kuwano A, Miyoshi O, Yamada K, Niikawa N, Tsukahara M. Sugio Y, et al. Am J Med Genet. 1998 Sep 23;79(3):191-4. doi: 10.1002/(sici)1096-8628(19980923)79:3<191::aid-ajmg7>3.0.co;2-q. Am J Med Genet. 1998. PMID: 9788559

4

Two Japanese cases with microcephalic primordial dwarfism: classical Seckel syndrome and osteodysplastic primordial dwarfism type II.

Sugio Y, Tsukahara M, Kajii T. Sugio Y, et al. Jpn J Hum Genet. 1993 Jun;38(2):209-17. doi: 10.1007/BF01883712. Jpn J Hum Genet. 1993. PMID: 8358044

5

New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardation.

Tsukahara M, Sugio Y. Tsukahara M, et al. Among authors: sugio y. J Hum Genet. 1998;43(4):224-7. doi: 10.1007/s100380050077. J Hum Genet. 1998. PMID: 9852671

6

Pachygyria, joint contractures, and facial abnormalities: a new lethal syndrome.

Tsukahara M, Sugio Y, Kajii T, Takahashi M, Hirota M, Kato H. Tsukahara M, et al. Among authors: sugio y. J Med Genet. 1990 Aug;27(8):532. doi: 10.1136/jmg.27.8.532. J Med Genet. 1990. PMID: 2213849 Free PMC article. No abstract available.

7

Spondylocostal dysostosis: report of three patients.

Ohashi H, Sugio Y, Kajii T. Ohashi H, et al. Among authors: sugio y. Jinrui Idengaku Zasshi. 1987 Dec;32(4):299-303. doi: 10.1007/BF01910285. Jinrui Idengaku Zasshi. 1987. PMID: 3331396 No abstract available.

8

46,X,i(Xq)/47,XX,+13 mosaicism.

Igarashi M, Tsukahara M, Sugio Y, Katayama K, Kajii T. Igarashi M, et al. Among authors: sugio y. Ann Genet. 1985;28(4):241-4. Ann Genet. 1985. PMID: 3879438

9

Giant hepatic granuloma caused by Bartonella henselae.

Murano I, Yoshii H, Kurashige H, Sugio Y, Tsukahara M. Murano I, et al. Among authors: sugio y. Pediatr Infect Dis J. 2001 Mar;20(3):319-20. doi: 10.1097/00006454-200103000-00023. Pediatr Infect Dis J. 2001. PMID: 11303841

10

Ruvalcaba syndrome: autosomal dominant inheritance.

Sugio Y, Kajii T. Sugio Y, et al. Am J Med Genet. 1984 Dec;19(4):741-53. doi: 10.1002/ajmg.1320190414. Am J Med Genet. 1984. PMID: 6517098

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