Teraoka M - Search Results

1

Assignment of SLC17A6 (alias DNPI), the gene encoding brain/pancreatic islet-type Na+-dependent inorganic phosphate cotransporter to human chromosome 11p14.3.

Aihara Y, Onda H, Teraoka M, Yokoyama Y, Seino Y, Kasuya H, Hori T, Tomura H, Inoue I, Kojima I, Takeda J. Aihara Y, et al. Among authors: teraoka m. Cytogenet Cell Genet. 2001;92(1-2):167-9. doi: 10.1159/000056893. Cytogenet Cell Genet. 2001. PMID: 11306821 No abstract available.

2

Maternal origin of a unique extra chromosome, der(9)(pter-->q13::q13-->q12:) in a girl with typical trisomy 9p syndrome.

Teraoka M, Narahara K, Yokoyama Y, Ninomiya S, Mizuta S, Une T, Seino Y. Teraoka M, et al. Am J Med Genet. 2001 Jul 22;102(1):25-8. doi: 10.1002/1096-8628(20010722)102:1<25::aid-ajmg1399>3.0.co;2-b. Am J Med Genet. 2001. PMID: 11471168

3

Cryptic pericentric inversion of chromosome 17 detected by fluorescence in situ hybridization study in familial Miller-Dieker syndrome.

Yokoyama Y, Narahara K, Teraoka M, Koyama K, Seino Y, Yagi S, Konishi T, Miyawaki T. Yokoyama Y, et al. Among authors: teraoka m. Am J Med Genet. 1997 Aug 8;71(2):236-7. doi: 10.1002/(sici)1096-8628(19970808)71:2<236::aid-ajmg24>3.0.co;2-e. Am J Med Genet. 1997. PMID: 9217231 No abstract available.

4

45,X/46,X,idic(Yq) mosaicism: clinical, cytogenetic, and molecular studies in four individuals.

Teraoka M, Narahara K, Yokoyama Y, Tsuji K, Kikkawa K, Ito S, Koyama K, Seino Y. Teraoka M, et al. Am J Med Genet. 1998 Aug 6;78(5):424-8. doi: 10.1002/(sici)1096-8628(19980806)78:5<424::aid-ajmg6>3.0.co;2-l. Am J Med Genet. 1998. PMID: 9714008

5

Two novel mutations of SURF1 in Leigh syndrome with cytochrome c oxidase deficiency.

Teraoka M, Yokoyama Y, Ninomiya S, Inoue C, Yamashita S, Seino Y. Teraoka M, et al. Hum Genet. 1999 Dec;105(6):560-3. doi: 10.1007/s004399900191. Hum Genet. 1999. PMID: 10647889

6

Rapid screening method to detect mutations in CYP21, the gene for 21-hydroxylase.

Yokoyama Y, Teraoka M, Tsuji K, Ninomiya S, Inoue C, Yamashita S, Narahara K, Seino Y. Yokoyama Y, et al. Among authors: teraoka m. Am J Med Genet. 2000 Sep 4;94(1):28-31. doi: 10.1002/1096-8628(20000904)94:1<28::aid-ajmg6>3.0.co;2-f. Am J Med Genet. 2000. PMID: 10982478

7

A novel mutation (296 del G) of the SOX90 gene in a patient with campomelic syndrome and sex reversal.

Ninomiya S, Yokoyama Y, Teraoka M, Mori R, Inoue C, Yamashita S, Tamai H, Funato M, Seino Y. Ninomiya S, et al. Among authors: teraoka m. Clin Genet. 2000 Sep;58(3):224-7. doi: 10.1034/j.1399-0004.2000.580310.x. Clin Genet. 2000. PMID: 11076045

8

Fatal neonatal mitochondrial cytopathy with disseminated fatty nodules in the liver.

Teraoka M, Yokoyama Y, Ichimura K, Mori R, Seino Y. Teraoka M, et al. Pediatr Int. 2003 Oct;45(5):570-3. doi: 10.1046/j.1442-200x.2003.01788.x. Pediatr Int. 2003. PMID: 14521534 No abstract available.

9

[Cat eye syndrome].

Teraoka M, Narahara K. Teraoka M, et al. Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):348-9. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11057256 Review. Japanese. No abstract available.

10

[Smith-Magenis syndrome].

Teraoka M, Narahara K. Teraoka M, et al. Ryoikibetsu Shokogun Shirizu. 1996;(15):224-6. Ryoikibetsu Shokogun Shirizu. 1996. PMID: 9047993 Review. Japanese. No abstract available.

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