Muroya K - Search Results

1

Short stature in a girl with partial monosomy of the pseudoautosomal region distal to DXYS15: further evidence for the assignment of the critical region for a pseudoautosomal growth gene(s).

Ogata T, Yoshizawa A, Muroya K, Matsuo N, Fukushima Y, Rappold G, Yokoya S. Ogata T, et al. Among authors: muroya k. J Med Genet. 1995 Oct;32(10):831-4. doi: 10.1136/jmg.32.10.831. J Med Genet. 1995. PMID: 8558568 Free PMC article.

2

Refinement of the locus for X-linked recessive chondrodysplasia punctata.

Muroya K, Ogata T, Rappold G, Klink A, Nakahori Y, Fukushima Y, Aizu K, Matsuo N. Muroya K, et al. Hum Genet. 1995 May;95(5):577-80. doi: 10.1007/BF00223874. Hum Genet. 1995. PMID: 7759082

3

Mental retardation in a boy with an interstitial deletion at Xp22.3 involving STS, KAL1, and OA1: implication for the MRX locus.

Muroya K, Ogata T, Matsuo N, Nagai T, Franco B, Ballabio A, Rappold G, Sakura N, Fukushima Y. Muroya K, et al. Am J Med Genet. 1996 Sep 6;64(4):583-7. doi: 10.1002/(SICI)1096-8628(19960906)64:4<583::AID-AJMG11>3.0.CO;2-D. Am J Med Genet. 1996. PMID: 8870926

4

Impaired male sex development in an infant with molecularly defined partial 9p monosomy: implication for a testis forming gene(s) on 9p.

Ogata T, Muroya K, Matsuo N, Hata J, Fukushima Y, Suzuki Y. Ogata T, et al. Among authors: muroya k. J Med Genet. 1997 Apr;34(4):331-4. doi: 10.1136/jmg.34.4.331. J Med Genet. 1997. PMID: 9138160 Free PMC article.

5

Microphthalmia with linear skin defects syndrome in a mosaic female infant with monosomy for the Xp22 region: molecular analysis of the Xp22 breakpoint and the X-inactivation pattern.

Ogata T, Wakui K, Muroya K, Ohashi H, Matsuo N, Brown DM, Ishii T, Fukushima Y. Ogata T, et al. Among authors: muroya k. Hum Genet. 1998 Jul;103(1):51-6. doi: 10.1007/s004390050782. Hum Genet. 1998. PMID: 9737776 Review.

6

Deletion mapping and X inactivation analysis of a non-specific mental retardation gene at Xp21.3-Xp22.11.

Muroya K, Kinoshita E, Kamimaki T, Matsuo N, Yorifugi T, Ogata T. Muroya K, et al. J Med Genet. 1999 Mar;36(3):187-91. J Med Genet. 1999. PMID: 10204842 Free PMC article.

7

Random X-inactivation in a girl with duplication Xp11.21-p21.3: report of a patient and review of the literature.

Matsuo M, Muroya K, Kosaki K, Ishii T, Fukushima Y, Anzo M, Ogata T. Matsuo M, et al. Among authors: muroya k. Am J Med Genet. 1999 Sep 3;86(1):44-50. Am J Med Genet. 1999. PMID: 10440827 Review.

8

Mother and daughter with 45,X/46,X,r(X)(p22.3q28) and mental retardation: analysis of the X-inactivation patterns.

Matsuo M, Muroya K, Nanao K, Hasegawa Y, Terasaki H, Kosaki K, Ogata T. Matsuo M, et al. Among authors: muroya k. Am J Med Genet. 2000 Apr 10;91(4):267-72. Am J Med Genet. 2000. PMID: 10766981 Review.

9

Structural analysis of a rare rearranged Y chromosome and its bearing on genotype-phenotype correlation.

Ogata T, Wakui K, Kosho T, Muroya K, Yamanouchi Y, Takano T, Fukushima Y, Rappold G, Suzuki Y. Ogata T, et al. Among authors: muroya k. Am J Med Genet. 2000 Jun 5;92(4):256-9. Am J Med Genet. 2000. PMID: 10842291

10

Clinical and molecular studies in 15 females with ring X chromosomes: implications for r(X) formation and mental development.

Matsuo M, Muroya K, Adachi M, Tachibana K, Asakura Y, Nakagomi Y, Hanaki K, Yokoya S, Yoshizawa A, Igarashi Y, Hanew K, Matsuo N, Ogata T. Matsuo M, et al. Among authors: muroya k. Hum Genet. 2000 Nov;107(5):433-9. doi: 10.1007/s004390000377. Hum Genet. 2000. PMID: 11140940

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

189 results

Search Page

Filters