Kawame H - Search Results

1

BAC array CGH reveals genomic aberrations in idiopathic mental retardation.

Miyake N, Shimokawa O, Harada N, Sosonkina N, Okubo A, Kawara H, Okamoto N, Kurosawa K, Kawame H, Iwakoshi M, Kosho T, Fukushima Y, Makita Y, Yokoyama Y, Yamagata T, Kato M, Hiraki Y, Nomura M, Yoshiura K, Kishino T, Ohta T, Mizuguchi T, Niikawa N, Matsumoto N. Miyake N, et al. Among authors: kawame h. Am J Med Genet A. 2006 Feb 1;140(3):205-11. doi: 10.1002/ajmg.a.31098. Am J Med Genet A. 2006. PMID: 16419101

2

Osteogenesis imperfecta-like syndrome with severe mental retardation and extrapyramidal tract signs.

Nishimura G, Kurosawa K, Kobayashi H, Kawame H. Nishimura G, et al. Among authors: kawame h. Pediatr Radiol. 1998 Nov;28(11):856-8. doi: 10.1007/s002470050482. Pediatr Radiol. 1998. PMID: 9799318 Review.

3

Syndrome of microcephaly, Dandy-Walker malformation, and Wilms tumor caused by mosaic variegated aneuploidy with premature centromere division (PCD): report of a new case and review of the literature.

Kawame H, Sugio Y, Fuyama Y, Hayashi Y, Suzuki H, Kurosawa K, Maekawa K. Kawame H, et al. J Hum Genet. 1999;44(4):219-24. doi: 10.1007/s100380050147. J Hum Genet. 1999. PMID: 10429359 Review.

4

Polymicrogyria is an uncommon manifestation in 22q11.2 deletion syndrome.

Kawame H, Kurosawa K, Akatsuka A, Ochiai Y, Mizuno K. Kawame H, et al. Am J Med Genet. 2000 Sep 4;94(1):77-8. doi: 10.1002/1096-8628(20000904)94:1<77::aid-ajmg16>3.0.co;2-v. Am J Med Genet. 2000. PMID: 10982488 No abstract available.

5

Functional disomy for Xq26.3-qter in a boy with an unbalanced t(X;21)(q26.3;p11.2) translocation.

Akiyama M, Kawame H, Ohashi H, Tohma T, Ohta H, Shishikura A, Miyata I, Usui N, Eto Y. Akiyama M, et al. Among authors: kawame h. Am J Med Genet. 2001 Mar 1;99(2):111-4. doi: 10.1002/1096-8628(2001)9999:9999<::aid-ajmg1150>3.0.co;2-c. Am J Med Genet. 2001. PMID: 11241467 Review.

6

Graves' disease in patients with 22q11.2 deletion.

Kawame H, Adachi M, Tachibana K, Kurosawa K, Ito F, Gleason MM, Weinzimer S, Levitt-Katz L, Sullivan K, McDonald-McGinn DM. Kawame H, et al. J Pediatr. 2001 Dec;139(6):892-5. doi: 10.1067/mpd.2001.119448. J Pediatr. 2001. PMID: 11743521

7

Patellar dislocation in Kabuki syndrome.

Kurosawa K, Kawame H, Ochiai Y, Nakashima M, Tohma T, Ohashi H. Kurosawa K, et al. Among authors: kawame h. Am J Med Genet. 2002 Mar 1;108(2):160-3. doi: 10.1002/ajmg.10247. Am J Med Genet. 2002. PMID: 11857567

8

[Analysis of 14 individuals who requested predictive genetic testing for hereditary neuromuscular diseases].

Yoshida K, Tamai M, Kubota T, Kawame H, Amano N, Ikeda S, Fukushima Y. Yoshida K, et al. Among authors: kawame h. Rinsho Shinkeigaku. 2002 Feb;42(2):113-7. Rinsho Shinkeigaku. 2002. PMID: 12424959 Japanese.

9

Further delineation of the behavioral and neurologic features in Costello syndrome.

Kawame H, Matsui M, Kurosawa K, Matsuo M, Masuno M, Ohashi H, Fueki N, Aoyama K, Miyatsuka Y, Suzuki K, Akatsuka A, Ochiai Y, Fukushima Y. Kawame H, et al. Am J Med Genet A. 2003 Apr 1;118A(1):8-14. doi: 10.1002/ajmg.a.10236. Am J Med Genet A. 2003. PMID: 12605434

10

Preferential paternal origin of microdeletions caused by prezygotic chromosome or chromatid rearrangements in Sotos syndrome.

Miyake N, Kurotaki N, Sugawara H, Shimokawa O, Harada N, Kondoh T, Tsukahara M, Ishikiriyama S, Sonoda T, Miyoshi Y, Sakazume S, Fukushima Y, Ohashi H, Nagai T, Kawame H, Kurosawa K, Touyama M, Shiihara T, Okamoto N, Nishimoto J, Yoshiura K, Ohta T, Kishino T, Niikawa N, Matsumoto N. Miyake N, et al. Among authors: kawame h. Am J Hum Genet. 2003 May;72(5):1331-7. doi: 10.1086/375166. Epub 2003 Apr 9. Am J Hum Genet. 2003. PMID: 12687502 Free PMC article.

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

121 results

Search Page