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G Nishimura

Showing results (181-190 of 388) with videos related to

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Journal of Human Genetics|February 1, 2007
A Japanese case of oto-palato-digital syndrome type II: an apparent lack of phenotype-genotype correlationT Kondoh, N Okamoto, N Norimatsu, et al.
Pediatric Radiology|April 16, 1998
A distinct subtype of "metatropic dysplasia variant" characterised by advanced carpal skeletal age and subluxation of the radial headsG Nishimura, M Satoh, T Aihara, et al.
American Journal of Medical Genetics|April 29, 1998
Previously undescribed spondyloepiphyseal dysplasia associated with craniosynostosis, cataracts, cleft palate, and mental retardation: report of four sibsG Nishimura, Y Fukushima, T Aihara, et al.
Magnetic Resonance in Medicine|February 11, 2010
In vivo high-resolution magnetic resonance skin imaging at 1.5 T and 3 TJoëlle K Barral, Neal K Bangerter, Bob S Hu, et al.
Magnetic Resonance in Medicine|November 23, 2013
Hadamard slice encoding for reduced-FOV diffusion-weighted imagingEmine Ulku Saritas, Daeho Lee, Tolga Çukur, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|April 14, 1999
A young infant with Goldbloom syndromeS Kuwashima, G Nishimura, A Harigaya, et al.
Molecular Syndromology|May 9, 2013
COL2A1 Mutation in Spondylometaphyseal Dysplasia Algerian TypeS Matsubayashi, M Ikema, Y Ninomiya, 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|May 26, 1999
New brittle bone disorder: report of a family with six affected individualsG Nishimura, N Haga, K Aoki, et al.
American Journal of Medical Genetics|December 30, 1996
New form of platyspondylic lethal chondrodysplasiaK Akaba, G Nishimura, M Hashimoto, et al.
Pageof 39

Showing results (181-190 of 388) with videos related to

Sort By:
Pageof 39
Journal of Human Genetics|February 1, 2007
A Japanese case of oto-palato-digital syndrome type II: an apparent lack of phenotype-genotype correlationT Kondoh, N Okamoto, N Norimatsu, et al.
Pediatric Radiology|April 16, 1998
A distinct subtype of "metatropic dysplasia variant" characterised by advanced carpal skeletal age and subluxation of the radial headsG Nishimura, M Satoh, T Aihara, et al.
American Journal of Medical Genetics|April 29, 1998
Previously undescribed spondyloepiphyseal dysplasia associated with craniosynostosis, cataracts, cleft palate, and mental retardation: report of four sibsG Nishimura, Y Fukushima, T Aihara, et al.
Magnetic Resonance in Medicine|February 11, 2010
In vivo high-resolution magnetic resonance skin imaging at 1.5 T and 3 TJoëlle K Barral, Neal K Bangerter, Bob S Hu, et al.
Magnetic Resonance in Medicine|November 23, 2013
Hadamard slice encoding for reduced-FOV diffusion-weighted imagingEmine Ulku Saritas, Daeho Lee, Tolga Çukur, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|April 14, 1999
A young infant with Goldbloom syndromeS Kuwashima, G Nishimura, A Harigaya, et al.
Molecular Syndromology|May 9, 2013
COL2A1 Mutation in Spondylometaphyseal Dysplasia Algerian TypeS Matsubayashi, M Ikema, Y Ninomiya, 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|May 26, 1999
New brittle bone disorder: report of a family with six affected individualsG Nishimura, N Haga, K Aoki, et al.
American Journal of Medical Genetics|December 30, 1996
New form of platyspondylic lethal chondrodysplasiaK Akaba, G Nishimura, M Hashimoto, et al.
Pageof 39