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American Journal of Medical Genetics|October 26, 1999
Association of microphthalmia with esophageal atresia: report of two new patients and review of the literatureK Imaizumi, T Ishii, J Kimura, et al.
American Journal of Medical Genetics|January 1, 1993
Balanced complex rearrangement involving chromosomes 8, 9, and 12 in a normal mother, derivative chromosome 9 with recombinant chromosome 12 in her daughter with minor anomaliesM Masuno, J Asano, K Yasuda, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|December 1, 1990
Two unrelated cases of single maxillary central incisor with 7q terminal deletionM Masuno, Y Fukushima, Y Sugio, et al.
The Japanese Journal of Human Genetics|September 1, 1992
Interstitial deletion of the long arm of chromosome 11: report of a case and review of the literatureA Wakazono, M Masuno, S Yamaguchi, et al.
Human Genetics|December 22, 1998
Alteration of the LIS1 gene in Japanese patients with isolated lissencephaly sequence or Miller-Dieker syndromeM Sakamoto, J Ono, S Okada, et al.
The Japanese Journal of Human Genetics|June 1, 1993
Interstitial deletion of the long arm of chromosome 11 determined by fluorescence in situ hybridizationT Hori, M Masuno, A Wakazono, et al.
Clinical Dysmorphology|January 29, 2000
Frontonasal dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation, and CNS structural anomalies: another observationM Masuno, K Imaizumi, N Aida, et al.
American Journal of Medical Genetics|January 24, 1998
Congenital scoliosis (hemivertebra) associated with de novo balanced reciprocal translocation, 46,XX,t(13;17)(q34;p11.2)K Imaizumi, M Masuno, T Ishii, et al.
Experimental Cell Research|August 1, 1992
Transformation and characterization of mutant human fibroblasts defective in peroxisome assemblyH Okamoto, Y Suzuki, N Shimozawa, et al.
American Journal of Medical Genetics|December 4, 1995
Miller-Dieker syndrome due to maternal cryptic translocation t(10;17) (q26.3;p13.3)M Masuno, K Imaizumi, M Nakamura, et al.
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