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YW

Yoshiharu Wakita

Okayama University

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Co-Authors

Kouji Narahara

Tsurumi University

Kiyoshi Kikkawa

CHI Health

Hiroshi Kimoto

National Society of Professional Engineers

Yukio Takahashi

Tohoku University

Shunsuke Kimura

St. Jude Children's Research Hospital

R. Kasai

Yokkaichi Municipal Hospital

Yuji Yokoyama

Okayama Psychiatric Medical Center

Masae Murakami

European Organisation for Research and Treatment of Cancer

Hiroshi Namba

Okayama University

Yusuke Himoto

Okayama University

Cooperative Institutions

Okayama University

Kyoto University

Tohoku University

National Center of Neurology and Psychiatry

Kobe University

Nagoya University

Kyushu University

Osaka University

Okayama Red Cross General Hospital

The University of Tokyo

Author Statistics

Papers

Citation

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Research Field

Improvement of Chromosome Definition in Grammatical Evolution

Civil-comp proceedings (2013)

Hideyuki Sugiura Yoshiharu Wakita Eisuke Kita

Grammatical evolution

10.4203/ccp.103.17

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Citations (0)

A variant Philadelphia chromosome (Ph1) positive chronic myelocytic leukemia.

Yuro Haruta Isamu Takahashi N Sekito K Miyamoto M Shimamoto

A rare case of variant Philadelphia (Ph1) chromosome positive [46, XX, t (9; 22) (q34; q11), inv (9) (9q22; 22q13)] chronic myelocytic leukemia (CML) was described. The patient, 73 years old female, was hospitalized to our hospital because of leukocytosis. Hematological findings corresponded to those of CMLs. However, this case lacked hepatosplenomegaly. Southern blot analysis using a 3 breakpoint cluster region (bcr) probe revealed a bcr rearrangement. The patient has been in the chronic phase for sixteen months without treatment. Clinical and chromosomal changes are under observation in order to get accumulate data for a pathophysiological analysis of variant Ph1 positive CMLs.

Leukocytosis

breakpoint cluster region

Hepatosplenomegaly

Myelocytic leukemia

Philadelphia chromosome

Breakpoint

10.18926/amo/30448

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Citations (0)

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

The Japanese Journal of Human Genetics (1985)

Yukio Takahashi Kouji Narahara Kiyoshi Kikkawa Yoshiharu Wakita Shunsuke Kimura

Long arm

Monosomy

Girl

10.1007/bf01907967

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Citations (16)

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

Human Genetics (1985)

Kouji Narahara Shunsuke Kimura Kiyoshi Kikkawa Yukio Takahashi Yoshiharu Wakita

Isocitrate dehydrogenase

Trisomy

Null allele

Heterozygote advantage

10.1007/bf00295665

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Citations (63)

The critical chromosome segment involved in 4p-syndrome: high resolution banding studies of five familial cases

Nihon Senten Ijo Gakkai kaiho/Senten ijō (1984)

K Narahara Yusuke Himoto Yuji Yokoyama R. Kasai Akira Hata

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Citations (0)

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

The Japanese Journal of Human Genetics (1985)

R. Kasai Kouji Narahara Kiyoshi Kikkawa Yukio Takahashi Yoshiharu Wakita

Chromosomal inversion

dup

Long arm

Chromosomal rearrangement

10.1007/bf01873578

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Citations (8)

De novo complex chromosome rearrangement in identical twins with multiple congenital anomalies

Human Genetics (1992)

Yoshiharu Wakita Kouji Narahara Kazushiro Tsuji Yuji Yokoyama Shinsuke Ninomiya

Chromosomal rearrangement

Breakpoint

Metabolic disease

Abnormality

10.1007/bf00219353

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Citations (13)

Duplication of 2p25: confirmation of the assignment of soluble acid phosphatase (ACP1) locus to 2p25

Human Genetics (1985)

Yoshiharu Wakita Kouji Narahara Yukio Takahashi Kiyoshi Kikkawa Shunsuke Kimura

10.1007/bf00284586

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Citations (19)

Pallister-Killian syndrome: Cytogenetic and biochemical studies

The Japanese Journal of Human Genetics (1988)

Kouji Narahara Yoshiharu Wakita Kiyoshi Kikkawa Kei Hiramoto Hiroshi Namba

Tetrasomy

Chromosome 12

10.1007/bf02032864

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Citations (12)

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

The Japanese Journal of Human Genetics (1984)

Kouji Narahara Yusuke Himoto Yuji Yokoyama R. Kasai Akira Hata

Microcephaly

Monosomy

Breakpoint

10.1007/bf01876498

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Citations (20)