Matsumoto T - Search Results

1

Chromosomal localisation of a pseudoautosomal growth gene(s).

Ogata T, Petit C, Rappold G, Matsuo N, Matsumoto T, Goodfellow P. Ogata T, et al. Among authors: matsumoto t. J Med Genet. 1992 Sep;29(9):624-8. doi: 10.1136/jmg.29.9.624. J Med Genet. 1992. PMID: 1404292 Free PMC article.

2

47,XX,UPD(7)mat,+r(7)pat/46,XX,UPD(7)mat mosaicism in a girl with Silver-Russell syndrome (SRS): possible exclusion of the putative SRS gene from a 7p13-q11 region.

Miyoshi O, Kondoh T, Taneda H, Otsuka K, Matsumoto T, Niikawa N. Miyoshi O, et al. Among authors: matsumoto t. J Med Genet. 1999 Apr;36(4):326-9. J Med Genet. 1999. PMID: 10227403 Free PMC article.

3

Complex glycerol kinase deficiency: molecular-genetic, cytogenetic, and clinical studies of five Japanese patients.

Matsumoto T, Kondoh T, Yoshimoto M, Fujieda K, Matsuura N, Matsuda I, Miike T, Yano K, Okuno A, Aoki Y, et al. Matsumoto T, et al. Am J Med Genet. 1988 Nov;31(3):603-16. doi: 10.1002/ajmg.1320310315. Am J Med Genet. 1988. PMID: 2852474 Review.

4

Allergic disease as an association of steroid sulphatase deficiency.

Sakura N, Nishimura S, Matsumoto T, Ohsaki M, Ogata T. Sakura N, et al. Among authors: matsumoto t. J Inherit Metab Dis. 1997 Nov;20(6):807-10. doi: 10.1023/a:1005375902993. J Inherit Metab Dis. 1997. PMID: 9427150

5

Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome.

Kubota T, Saitoh S, Matsumoto T, Narahara K, Fukushima Y, Jinno Y, Niikawa N. Kubota T, et al. Among authors: matsumoto t. Am J Med Genet. 1994 Feb 15;49(4):378-83. doi: 10.1002/ajmg.1320490405. Am J Med Genet. 1994. PMID: 7909196

6

Two cases of steroid sulfatase deficiency with complex phenotype due to contiguous gene deletions.

Nishimura S, Masuda H, Matsumoto T, Sakura N, Matsumoto T, Ueda K. Nishimura S, et al. Among authors: matsumoto t. Am J Med Genet. 1991 Sep 1;40(3):260-3. doi: 10.1002/ajmg.1320400303. Am J Med Genet. 1991. PMID: 1951426

7

The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32.

Fujimoto M, Kantaputra PN, Ikegawa S, Fukushima Y, Sonta S, Matsuo M, Ishida T, Matsumoto T, Kondo S, Tomita H, Deng HX, D'urso M, Rinaldi MM, Ventruto V, Takagi T, Nakamura Y, Niikawa N. Fujimoto M, et al. Among authors: matsumoto t. J Hum Genet. 1998;43(1):32-6. doi: 10.1007/s100380050033. J Hum Genet. 1998. PMID: 9609995

8

Origin of the extra chromosome in trisomy 18. A study on five patients using a restriction fragment length polymorphism.

Kondoh T, Tonoki H, Matsumoto T, Tsukahara M, Niikawa N. Kondoh T, et al. Among authors: matsumoto t. Hum Genet. 1988 Aug;79(4):377-8. doi: 10.1007/BF00282181. Hum Genet. 1988. PMID: 2900802

9

Two sisters with clinical diagnosis of Wiskott-Aldrich syndrome: is the condition in the family autosomal recessive?

Kondoh T, Hayashi K, Matsumoto T, Yoshimoto M, Morio T, Yata J, Tsuji Y. Kondoh T, et al. Among authors: matsumoto t. Am J Med Genet. 1995 Oct 9;60(5):364-9. doi: 10.1002/ajmg.1320600504. Am J Med Genet. 1995. PMID: 8546147

10

Origin and mechanism of formation of 45,X/47,XX,+21 mosaicism in a fetus.

Harada N, Abe K, Nishimura T, Sasaki K, Ishikawa M, Fujimoto M, Matsumoto T, Niikawa N. Harada N, et al. Among authors: matsumoto t. Am J Med Genet. 1998 Feb 3;75(4):432-7. doi: 10.1002/(sici)1096-8628(19980203)75:4<432::aid-ajmg17>3.0.co;2-p. Am J Med Genet. 1998. PMID: 9482654

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

10,254 results

Search Page

Filters