R. Kasai

发表

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

K. Narahara, Y. Takahashi, K. Kikkawa, 2004, Human Genetics.

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

A. Hata, K. Narahara, Y. Yokoyama, 1984, Japanese Journal of Human Genetics.

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

Y. Fukushima, K. Narahara, K. Wakui, 1991, American journal of medical genetics.

Pallister-Killian syndrome: Cytogenetic and biochemical studies

K. Narahara, K. Kikkawa, K. Hiramoto, 1988, Japanese Journal of Human Genetics.

A Patient with Ring 9 Chromosome 46, XY, r(9)(p24.1q34.3)

R. Kasai, N. Kasa, 1988, Acta paediatrica Japonica : Overseas edition.

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

K. Narahara, K. Kikkawa, M. Murakami, 1985, The Japanese Journal of Human Genetics.

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

K. Narahara, K. Kikkawa, R. Kasai, 2004, Human Genetics.

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

K. Narahara, K. Kikkawa, S. Kimura, 1985, Japanese Journal of Human Genetics.

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)

K. Narahara, Y. Yokoyama, K. Hiramoto, 1989, Japanese Journal of Human Genetics.