I. Teshima

发表

Tissue-specific methylation differences and cognitive function in fragile X premutation females.

D. Chitayat, D. Allingham-Hawkins, P. Ray, 1996, American journal of medical genetics.

Velo-cardio-facial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders.

C. Cytrynbaum, R. Schachar, P. Arnold, 2001, American journal of medical genetics.

FISH detection of chromosome 15 deletions in Prader-Willi and Angelman syndromes.

R. Weksberg, D. Chitayat, C. Shuman, 1996, American journal of medical genetics.

Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)].

V. Jay, D. Chitayat, L. Becker, 1996, American journal of medical genetics.

Peripheral Medulloepithelioma: An Immunohistochemical, Ultrastructural, and Cytogenetic Study of a Rare, Chemotherapy-Sensitive, Pediatric Tumor

L. Donner, I. Teshima, 2003, The American journal of surgical pathology.

Omphalocele in Miller-Dieker syndrome: expanding the phenotype.

D. Chitayat, A. Toi, S. Blaser, 1997, American journal of medical genetics.

Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies.

V. Jay, A. James, D. Chitayat, 1998, American journal of medical genetics.

Wilms tumor in a patient with Prader-Willi syndrome.

D. Ledbetter, R. Weksberg, M. Coppes, 1993, The Journal of pediatrics.

Physical mapping of probes within 14q32, a subtelomeric region showing a high recombination frequency.

Y. Nakamura, R. White, D. Cox, 1990, Genomics.

Malignant hematological disorders in children with Wolf–Hirschhorn syndrome

D. Chitayat, M. Freedman, A. Sharathkumar, 2003, American journal of medical genetics. Part A.

Monozygotic twins with 45,X/46,XY mosaicism discordant for phenotypic sex.

P. Ray, T. Costa, I. Teshima, 1998, American journal of medical genetics.

Array‐based genomic delineation of a familial duplication 11q14.1–q22.1 associated with recurrent depression

D. Chitayat, T. Ben-Omran, Jillian Murphy, 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genetic analysis of patients with the Saethre-Chotzen phenotype.

S. Scherer, W. Meschino, P. Ray, 2002, American journal of medical genetics.

Late‐appearing Philadelphia chromosome in childhood acute myeloid leukemia

S. Baruchel, M. Abdelhaleem, I. Teshima, 2008, Pediatric blood & cancer.

Intrascrotal lipoblastoma with a complex karyotype: a case report and review of the literature.

G. Taylor, A. Khoury, G. Somers, 2004, Archives of pathology & laboratory medicine.

Response to correspondence from Gripp et al.—“clinical and molecular diagnosis should be consistent”

A. Teebi, K. Chun, I. Teshima, 2003, American journal of medical genetics. Part A.

Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome.

S. Scherer, B. Fernandez, R. Weksberg, 2002, Genomics.

Mosaicism for duplication 12q (12ql3-+q24.2) in a dysmorphic male infant

T. Costa, I. Teshima, J. Dixon, 2022 .

A der(19)t(12;19)(q12;p13.3) in a case of pediatric acute leukemia with unusual immunophenotype.

M. Abdelhaleem, I. Teshima, C. Ye, 2005, Cancer genetics and cytogenetics.

An active ring X and haploinsufficiency of SHOX contribute to short stature, congenital anomalies, and developmental delay in a female.

M. Shago, D. Chitayat, P. Chakraborty, 2002, American journal of medical genetics.

Association of the t(12;22)(q13;q12) EWS/ATF1 Rearrangement With Polyphenotypic Round Cell Sarcoma of Bone: A Case Report

P. Nathan, M. Zielenska, G. Somers, 2005, The American journal of surgical pathology.

Transabdominal chorionic villus sampling in the second trimester.

C. Høgdall, I. Teshima, J. Shime, 1988, American journal of obstetrics and gynecology.

Deletion 4q21/4q22 syndrome: two patients with de novo 4q21.3q23 and 4q13.2q23 deletions.

M. Nowaczyk, J. Clarke, I. Teshima, 1997, American journal of medical genetics.

Holoprosencephaly and cleidocranial dysplasia in a patient due to two position‐effect mutations: case report and review of the literature

J. Herbrick, I. Teshima, J. Siegel‐Bartelt, 2005, Clinical genetics.

Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2

Jessica Brian, Wendy Roberts, Lars Feuk, 2006, American journal of medical genetics. Part A.

Speech and Language Impairment and Oromotor Dyspraxia Due to Deletion of 7 q 31 That Involves FOXP 2

Stephen W. Scherer, Lucy R. Osborne, Jessica Brian, 2006 .

Primary Ewing’s Sarcoma of the Skull in Children

J. Drake, J. Rutka, L. Becker, 1999, Pediatric Neurosurgery.

Analysis of chromosome 22q as an aid to the diagnosis of rhabdoid tumor: a case report.

J. Squire, G. Taylor, P. Thorner, 1999, The American journal of surgical pathology.

Canadian multicenter randomized clinical trial of chorion villus sampling and amniocentesis. chromosome mosaicism in CVS and amniocentesis samples.

M. Vekemans, R. Gagné, D. Kalousek, 1992, Prenatal diagnosis.

Genes for immunoglobulin heavy chains and for α1-antitrypsin are localized to specific regions of chromosome 14q

D. Cox, I. Teshima, V. Markovic, 1982, Nature.

Human Chromosome 7: DNA Sequence and Biology

Junjun Zhang, Nazneen Rahman, Alexander K. Hudek, 2003, Science.

Detecting rearrangements in children using subtelomeric FISH and SKY.

R. Weksberg, S. Meyn, A. Teebi, 2002, American journal of medical genetics.

Patients with deletions of 9q22q34 do not define a syndrome: three case reports and a literature review

S. Farrell, I. Teshima, J. Siegel‐Bartelt, 1991, Clinical genetics.

Localization and genetic linkage of the human immunoglobulin heavy chain genes and the creatine kinase brain (CKB) gene: identification of a hot spot for recombination.

M. Walter, D. Cox, G. Daouk, 1991, Genomics.

Interstitial deletion of 1p22.2p31.1 and medium‐chain acyl‐CoA dehydrogenase deficiency in a patient with global developmental delay

B. Andresen, N. Poplawski, J. Clarke, 2008, American journal of medical genetics. Part A.

Craniosynostosis associated with partial duplication of 15q and deletion of 2q.

A. Feigenbaum, M. V. Van Allen, I. Teshima, 1992, American journal of medical genetics.

Inherited duplication, dup (8) (p23.1p23.1) pat, in a father and daughter with congenital heart defects.

A. Teebi, I. Adatia, I. Teshima, 2001, American journal of medical genetics.

Hunter disease (mucopolysaccharidosis type II) in a karyotypically normal girl

H. Willard, J. Clarke, I. Teshima, 1990, Clinical genetics.

Use of Multicolor Spectral Karyotyping in Genetic Analysis of Pleuropulmonary Blastoma

J. Squire, J. Bayani, P. Thorner, 2000, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Echocardiographic evaluation of the spectrum of cardiac anomalies associated with trisomy 13 and trisomy 18.

J. Smallhorn, R. Freedom, I. Teshima, 1990, Journal of the American College of Cardiology.

4.3‐Mb triplication of 4q32.1–q32.2: Report of a family through two generations

Jia-chi Wang, I. Teshima, Małgorzata J. M. Nowaczyk, 2009, American journal of medical genetics. Part A.

Molecular analysis redefines three human chromosome 14 deletions

R. Haslam, D. Cox, R. Wintle, 1995, Human Genetics.

Clinical Report Interstitial Deletion of 1p22.2p31.1 and Medium-Chain Acyl-CoA Dehydrogenase Deficiency in a Patient With Global Developmental Delay

B. Andresen, N. Poplawski, I. Teshima, 2008 .

Central neurocytoma: morphological, flow cytometric, polymerase chain reaction, fluorescence in situ hybridization, and karyotypic analyses. Case report.

V. Jay, L. Becker, E. Hoving, 1999, Journal of neurosurgery.

Ring chromosome 22 and autism: report and review.

P. Szatmari, M. Nowaczyk, J. MacLean, 2000, American journal of medical genetics.

Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literature.

D. Chitayat, M. Vekemans, J. Posnick, 1995, American journal of medical genetics.

Total Resection of an Intracerebral Hemangioendothelioma in an Infant

M. Hodaie, L. Becker, J. Rutka, 2001, Pediatric Neurosurgery.

Microdeletion 22q11.2: clinical data and deletion size

C. Cytrynbaum, T. Scheidl, B. Emanuel, 1997, Journal of medical genetics.

Unique insertional translocation in a childhood Wilms' tumor survivor detected when his daughter developed bilateral retinoblastoma

B. Gallie, E. Héon, J. Sutherland, 2003, American journal of medical genetics. Part A.

Deletion 3q in two patients with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES).

M. Huggins, T. Costa, I. Teshima, 1998, Journal of pediatric ophthalmology and strabismus.

Molecular analysis of three patients with interstitial deletions of chromosome band 14q31.

N. Carter, D. Cox, I. Teshima, 1995, Journal of medical genetics.

Molecular analysis ofthree patients with interstitial deletions ofchromosome band 14q31

D. Cox, I. Teshima, W. Wilson, 1995 .

Annex 6: Chromosome mosaicism in CVS and amniocentesis samples

M. Vekemans, R. Gagné, M. Vekemans, 1992 .