Kasai R - Search Results

1

Probable assignment of soluble isocitrate dehydrogenase (IDH1) to 2q33.3.

Narahara K, Kimura S, Kikkawa K, Takahashi Y, Wakita Y, Kasai R, Nagai S, Nishibayashi Y, Kimoto H. Narahara K, et al. Among authors: kasai r. Hum Genet. 1985;71(1):37-40. doi: 10.1007/BF00295665. Hum Genet. 1985. PMID: 3861566

2

Reproductive risk of paracentric inversion carriers: report of two unrelated cases with paracentric inversion of the long arm of chromosome 3.

Kasai R, Narahara K, Kikkawa K, Takahashi Y, Wakita Y, Kimura S, Kataoka N, Kimoto H. Kasai R, et al. Jinrui Idengaku Zasshi. 1985 Jun;30(2):57-67. doi: 10.1007/BF01873578. Jinrui Idengaku Zasshi. 1985. PMID: 3841372 No abstract available.

3

Interstitial deletion of the long arm of chromosome 2: a case report and review of the literature.

Takahashi Y, Narahara K, Kikkawa K, Wakita Y, Kimura S, Murakami M, Kasai R, Kimoto H. Takahashi Y, et al. Among authors: kasai r. Jinrui Idengaku Zasshi. 1985 Dec;30(4):297-305. doi: 10.1007/BF01907967. Jinrui Idengaku Zasshi. 1985. PMID: 3869838 No abstract available.

4

Regional mapping of catalase and Wilms tumor--aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305----p1306.

Narahara K, Kikkawa K, Kimira S, Kimoto H, Ogata M, Kasai R, Hamawaki M, Matsuoka K. Narahara K, et al. Among authors: kasai r. Hum Genet. 1984;66(2-3):181-5. doi: 10.1007/BF00286597. Hum Genet. 1984. PMID: 6325323

5

The critical monosomic segment involved in 4p- syndrome: a high-resolution banding study on five inherited cases.

Narahara K, Himoto Y, Yokoyama Y, Kasai R, Hata A, Kikkawa K, Takahashi Y, Wakita Y, Kimura S, Kimoto H. Narahara K, et al. Among authors: kasai r. Jinrui Idengaku Zasshi. 1984 Dec;29(4):403-13. doi: 10.1007/BF01876498. Jinrui Idengaku Zasshi. 1984. PMID: 6535856 No abstract available.

6

Mapping of genes encoding coagulation factors VII and X to the distal portion of the 13q34 by gene dose study in a patient with r(13).

Kasai R, Narahara K, Namba H, Tsuji K, Matsubara T, Hiramoto K, Yokoyama Y, Kimoto H. Kasai R, et al. Jinrui Idengaku Zasshi. 1989 Sep;34(3):247-50. doi: 10.1007/BF01900729. Jinrui Idengaku Zasshi. 1989. PMID: 2634139 No abstract available.

7

Pallister-Killian syndrome: cytogenetic and biochemical studies.

Narahara K, Wakita Y, Kikkawa K, Hiramoto K, Namba H, Murakami M, Kasai R, Kimoto H. Narahara K, et al. Among authors: kasai r. Jinrui Idengaku Zasshi. 1988 Sep;33(3):339-47. doi: 10.1007/BF02032864. Jinrui Idengaku Zasshi. 1988. PMID: 3204687 No abstract available.

8

Specification of small distal 6q deletions in two patients by gene dosage and in situ hybridization study of plasminogen and alpha-L-fucosidase 2.

Narahara K, Tsuji K, Yokoyama Y, Namba H, Murakami M, Matsubara T, Kasai R, Fukushima Y, Seki T, Wakui K, et al. Narahara K, et al. Among authors: kasai r. Am J Med Genet. 1991 Sep 1;40(3):348-53. doi: 10.1002/ajmg.1320400322. Am J Med Genet. 1991. PMID: 1951444

9

Influence of CYP2C19 polymorphism and concomitant antiepileptic drugs on serum clobazam and N-desmethyl clobazam concentrations in patients with epilepsy.

Yamamoto Y, Takahashi Y, Imai K, Miyakawa K, Nishimura S, Kasai R, Ikeda H, Takayama R, Mogami Y, Yamaguchi T, Terada K, Matsuda K, Inoue Y, Kagawa Y. Yamamoto Y, et al. Among authors: kasai r. Ther Drug Monit. 2013 Jun;35(3):305-12. doi: 10.1097/FTD.0b013e318283b49a. Ther Drug Monit. 2013. PMID: 23666564

10

A patient with ring 9 chromosome 46,XY,r(9)(p24.1q34.3).

Kasa N, Kasai R. Kasa N, et al. Among authors: kasai r. Acta Paediatr Jpn. 1988 Dec;30(6):710-3. doi: 10.1111/j.1442-200x.1988.tb02558.x. Acta Paediatr Jpn. 1988. PMID: 3149132 No abstract available.

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