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Human Genetics|May 1, 1991
Replication asynchrony between homologs 15q11.2: cytogenetic evidence for genomic imprintingY Izumikawa, K Naritomi, K Hirayama
American Journal of Medical Genetics|June 15, 1993
Inverted insertion of chromosome 7q and ectrodactylyK Naritomi, Y Izumikawa, T Tohma, et al.
The Japanese Journal of Human Genetics|April 30, 1998
Characterization of marker chromosomes by fish using microdissected probes from old Carnoy-fixed cells: report of two casesY Chinen, T Tohma, Y Izumikawa, et al.
The Japanese Journal of Human Genetics|September 1, 1993
The Costello syndrome: a boy with thick mitral valves and arrhythmiasY Izumikawa, K Naritomi, T Tohma, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|June 1, 1989
Application of personal computer to an analysis of small de novo chromosomal insertion: a case of de novo 3q2 trisomy with ins(8;3)K Naritomi, Y Izumikawa, N Kinjo, et al.
Clinical Genetics|April 1, 1989
Trisomy 9q3 syndrome: a case report and review of the literatureK Naritomi, Y Izumikawa, Y Goya, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Assignment of the human PAX4 gene to chromosome band 7q32 by fluorescence in situ hybridizationT Tamura, Y Izumikawa, T Kishino, et al.
The Japanese Journal of Human Genetics|September 1, 1996
Small interstitial deletion of the long arm of chromosome 2 (2q24.3): further delineation of 2q medial monosomy syndromeY Chinen, T Tohma, Y Izumikawa, et al.
Clinical Genetics|May 1, 1988
16q21 is critical for 16q deletion syndromeK Naritomi, N Shiroma, Y Izumikawa, et al.
American Journal of Medical Genetics|July 15, 1992
Combined Goltz and Aicardi syndromes in a terminal Xp deletion: are they a contiguous gene syndrome?K Naritomi, Y Izumikawa, S Nagataki, et al.
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