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I Teshima

Showing results (11-20 of 28) with videos related to

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Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|July 13, 2000
Use of multicolor spectral karyotyping in genetic analysis of pleuropulmonary blastomaM Barnard, J Bayani, R Grant, et al.
Genomics|December 1, 1990
Molecular characterization of Beckwith-Wiedemann syndrome (BWS) patients with partial duplication of chromosome 11p excludes the gene MYOD1 from the BWS regionR Weksberg, M Glaves, I Teshima, et al.
Journal of Dental Research|June 5, 2009
Degradation-stage effect of self-etching primer on dentin bond durabilityM Aida, M Odaki, K Fujita, et al.
Clinical Genetics|May 1, 1990
Hunter disease (mucopolysaccharidosis type II) in a karyotypically normal girlJ T Clarke, H F Willard, I Teshima, et al.
Journal of Neurosurgery|February 9, 1999
Central neurocytoma: morphological, flow cytometric, polymerase chain reaction, fluorescence in situ hybridization, and karyotypic analyses. Case reportV Jay, V Edwards, E Hoving, et al.
American Journal of Medical Genetics|February 5, 1998
Monozygotic twins with 45,X/46,XY mosaicism discordant for phenotypic sexT Costa, M Lambert, I Teshima, et al.
The American Journal of Surgical Pathology|August 6, 1999
Analysis of chromosome 22q as an aid to the diagnosis of rhabdoid tumor: a case reportJ Simons, I Teshima, M Zielenska, et al.
Journal of the American College of Cardiology|March 1, 1990
Echocardiographic evaluation of the spectrum of cardiac anomalies associated with trisomy 13 and trisomy 18N N Musewe, D J Alexander, I Teshima, et al.
Genomics|January 1, 1990
Physical mapping of probes within 14q32, a subtelomeric region showing a high recombination frequencyM H Hofker, S Smith, Y Nakamura, et al.
Clinical Genetics|September 7, 2005
Holoprosencephaly and cleidocranial dysplasia in a patient due to two position-effect mutations: case report and review of the literatureB A Fernandez, J Siegel-Bartelt, J-A S Herbrick, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|July 13, 2000
Use of multicolor spectral karyotyping in genetic analysis of pleuropulmonary blastomaM Barnard, J Bayani, R Grant, et al.
Genomics|December 1, 1990
Molecular characterization of Beckwith-Wiedemann syndrome (BWS) patients with partial duplication of chromosome 11p excludes the gene MYOD1 from the BWS regionR Weksberg, M Glaves, I Teshima, et al.
Journal of Dental Research|June 5, 2009
Degradation-stage effect of self-etching primer on dentin bond durabilityM Aida, M Odaki, K Fujita, et al.
Clinical Genetics|May 1, 1990
Hunter disease (mucopolysaccharidosis type II) in a karyotypically normal girlJ T Clarke, H F Willard, I Teshima, et al.
Journal of Neurosurgery|February 9, 1999
Central neurocytoma: morphological, flow cytometric, polymerase chain reaction, fluorescence in situ hybridization, and karyotypic analyses. Case reportV Jay, V Edwards, E Hoving, et al.
American Journal of Medical Genetics|February 5, 1998
Monozygotic twins with 45,X/46,XY mosaicism discordant for phenotypic sexT Costa, M Lambert, I Teshima, et al.
The American Journal of Surgical Pathology|August 6, 1999
Analysis of chromosome 22q as an aid to the diagnosis of rhabdoid tumor: a case reportJ Simons, I Teshima, M Zielenska, et al.
Journal of the American College of Cardiology|March 1, 1990
Echocardiographic evaluation of the spectrum of cardiac anomalies associated with trisomy 13 and trisomy 18N N Musewe, D J Alexander, I Teshima, et al.
Genomics|January 1, 1990
Physical mapping of probes within 14q32, a subtelomeric region showing a high recombination frequencyM H Hofker, S Smith, Y Nakamura, et al.
Clinical Genetics|September 7, 2005
Holoprosencephaly and cleidocranial dysplasia in a patient due to two position-effect mutations: case report and review of the literatureB A Fernandez, J Siegel-Bartelt, J-A S Herbrick, et al.
Pageof 3