Author

Yoshimitsu Fukushima

Observed names: Y Fukushima, Y. FUKUSHIMA, Y. Fukushima

Institutions: Shinshu University, Shinshu University Hospital

Observed institutions: Dokkyo University, TEPCO (Japan), Asahikawa Medical College Hospital, Shinshu University, Asahikawa Medical University, Keio University, Hokkaido University, University of Michigan, Aomori Prefectural Central Hospital, Saitama Children's Medical Center, Michigan Medicine, Shimane Prefectural Central Hospital, Shinshu University Hospital, Nagasaki University, Shimane Medical University

OpenAlex ID: A5111835465

The 11q;22q translocation: A collaborative study of 20 new cases and analysis of 110 families

1983 · L. Iselius, J. Lindsten, et al. · Human Genetics · 190

GATA3 abnormalities and the phenotypic spectrum of HDR syndrome

2001 · Koji Muroya, Tomonobu Hasegawa, et al. · Journal of Medical Genetics · 162

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DNA deletion and its parental origin in Angelman syndrome patients

1991 · Jun‐Ichi Hamabe, Yoshikazu Kuroki, et al. · American Journal of Medical Genetics · 97

The proportion of cells with functional X disomy is associated with the severity of mental retardation in mosaic ring X Turner syndrome females

2002 · T. Kubota, K. Wakui, et al. · Cytogenetic and Genome Research · 49

EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) with a balanced reciprocal translocation between 7q11.21 and 9p12 (or 7p11.2 and 9q12) in three generations

1991 · Tomonobu Hasegawa, Yukihiro Hasegawa, et al. · Clinical Genetics · 44

Impaired male sex development in an infant with molecularly defined partial 9p monosomy: implication for a testis forming gene(s) on 9p.

1997 · T Ogata, K Muroya, et al. · Journal of Medical Genetics · 39

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Microcephaly and early-onset nephrotic syndrome ?confusion in Galloway-Mowat syndrome

1995 · Hitomi Sano, Akihiko Miyanoshita, et al. · Pediatric Nephrology · 32

Chromosome abnormalities involving 11p13 and low erythrocyte catalase activity

1982 · N. Niikawa, Y. Fukushima, et al. · Human Genetics · 22

Pseudoachondroplasia with de novo deletion [del(11)(q21q22.2)]

1998 · Shiro Ikegawa, Hirofumi Ohashi, et al. · American Journal of Medical Genetics · 15

Hypomelanosis of lto associated with neuroblastoma

1996 · E. Oguma, T. Aihara, et al. · Pediatric Radiology · 15

Ring chromosome 15 syndrome in an adult female

1996 · T. Matsuishi, Y. Yamada, et al. · Journal of Intellectual Disability Research · 4

Radiological changes of frontometaphyseal dysplasia in the neonate

1995 · G. Nishimura, H. Takano, et al. · Pediatric Radiology · 4

Woman with UV hypersensitivity and a de novo unbalanced chromosome translocation

2001 · Keiko Akahoshi, Shin-Ichi Moriwaki, et al. · American Journal of Medical Genetics · 2

DNA deletion in patients with von Recklinghausen neurofibromatosis

1992 · T. Kamei, Y. Fukushima, et al. · Clinical Genetics · 2

Tetramelic mirror-image like polydactyly and de novo balanced autosomal translocation, 46,XY,t(2;14)(p23.2;q13) : The 35th Annual Meeting of the Japanese Teratology Society

1995 · Hirofumi Ohashi, M. Iwamura, et al. · Congenital Anomalies · 1

Linkage Analysis of Mesomelic Dysplasia, Kantaputra Type

2001 · P. N. KANTAPUTRA, M. FUJIMOTO, et al. · WORLD SCIENTIFIC eBooks

[Septo-optic dysplasia].

2001 · A Sakurai, Y Fukushima · PubMed

[Pentalogy of Cantrell].

2001 · S Ishida, Y Fukushima · PubMed

[Pharynx/larynx hypoplasia-omphalocele, Shprintzen-Goldberg type].

2001 · S Ishida, Y Fukushima · PubMed

Sex chromosome abnormalities and X chromosome inactivation : Abstracts of Papers Presented at the Thirty-Third Annual Meeting of the Japanese Teratology Society Nagoya, Japan, July 21-23, 1993

1993 · Y. Fukushima · Congenital Anomalies

A patient associated with mirror hand, omphalocele, Morgagni hernia and hypoplastic pectoral muscle : A lateral plate mesoderm disruption sequence? : Abstracts of Papers Presented at the Thirty-Third Annual Meeting of the Japanese Teratology Society Nagoya, Japan, July 21-23, 1993

1993 · Hidenori Ohashi, M. Matsumoto, et al. · Congenital Anomalies

Works count: 21

Citation count: 678

H-index: 10

I10-index: 10