Matsumoto T - Search Results

1

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

2

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

3

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.

4

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

5

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

6

Molecular analysis of a patient with Beckwith-Wiedemann syndrome, rhabdomyosarcoma and renal cell carcinoma.

Matsumoto T, Kinoshita E, Maeda H, Niikawa N, Kurosaki N, Harada N, Yun K, Sawai T, Aoki S, Kondoh T, et al. Matsumoto T, et al. Jpn J Hum Genet. 1994 Jun;39(2):225-34. doi: 10.1007/BF01876842. Jpn J Hum Genet. 1994. PMID: 8086640

7

Regional mapping of the parathyroid hormone gene (PTH) by cytogenetic and molecular studies.

Tonoki H, Narahara K, Matsumoto T, Niikawa N. Tonoki H, et al. Among authors: matsumoto t. Cytogenet Cell Genet. 1991;56(2):103-4. doi: 10.1159/000133059. Cytogenet Cell Genet. 1991. PMID: 1672845

8

Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.

Sugino S, Fujishita S, Kamimura N, Matsumoto T, Wapenaar MC, Deng HX, Shibuya N, Miike T, Niikawa N. Sugino S, et al. Among authors: matsumoto t. Am J Med Genet. 1989 Dec;34(4):555-61. doi: 10.1002/ajmg.1320340421. Am J Med Genet. 1989. PMID: 2576185

9

Case of 46,XX/47,XY, +21 chimerism in a newborn infant with ambiguous genitalia.

Sawai T, Yoshimoto M, Kinoshita E, Baba T, Matsumoto T, Tsuji Y, Fukuda S, Harada N, Niikawa N. Sawai T, et al. Among authors: matsumoto t. Am J Med Genet. 1994 Feb 15;49(4):428-30. doi: 10.1002/ajmg.1320490415. Am J Med Genet. 1994. PMID: 8160738

10

Autosomal dominant onychodystrophy and congenital sensorineural deafness.

Kondoh T, Tsuru A, Matsumoto T, Matsuzaka T, Tsuji Y. Kondoh T, et al. Among authors: matsumoto t. J Hum Genet. 1999;44(1):60-2. doi: 10.1007/s100380050109. J Hum Genet. 1999. PMID: 9929981

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