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تسجيل الدخول للوصول الكامل.

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

المؤلفون: Burnside RD; Department of Cytogenetics, Laboratory Corporation of America, Center for Molecular Biology and Pathology, Research Triangle Park, NC 27709, USA. burnsir@labcorp.com, Pappas JG, Sacharow S, Applegate C, Hamosh A, Gadi IK, Jaswaney V, Keitges E, Phillips KK, Potluri VR, Risheg H, Smith JL, Tepperberg JH, Schwartz S, Papenhausen P

المصدر: American journal of medical genetics. Part A [Am J Med Genet A] 2013 Apr; Vol. 161A (4), pp. 822-8. Date of Electronic Publication: 2013 Mar 12.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

مواضيع طبية MeSH: Chromosome Deletion* , Phenotype*, Heart Defects, Congenital/*genetics, Abnormalities, Multiple/genetics ; Adult ; Child, Preschool ; Chromosomes, Human, Pair 8 ; Facies ; Female ; GATA4 Transcription Factor/genetics ; Genome-Wide Association Study ; Heart Defects, Congenital/diagnosis ; Humans ; Male ; Microsatellite Repeats ; Polymorphism, Single Nucleotide ; User-Computer Interface

SCR Disease Name: Chromosome 8, monosomy 8p

المؤلفون: Burnside RD; Laboratory Corporation of America, 1904 Alexander Dr., Research Triangle Park, NC 27709, USA. burnsir@labcorp.com, Pasion R, Mikhail FM, Carroll AJ, Robin NH, Youngs EL, Gadi IK, Keitges E, Jaswaney VL, Papenhausen PR, Potluri VR, Risheg H, Rush B, Smith JL, Schwartz S, Tepperberg JH, Butler MG

المصدر: Human genetics [Hum Genet] 2011 Oct; Vol. 130 (4), pp. 517-28. Date of Electronic Publication: 2011 Feb 27.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE

مواضيع طبية MeSH: Chromosome Deletion* , Gene Duplication*, Adaptor Proteins, Signal Transducing/*genetics , Chromosomes, Human, Pair 15/*genetics , Developmental Disabilities/*genetics , Language Development Disorders/*genetics , Mental Disorders/*genetics, Adolescent ; Adult ; Angelman Syndrome/genetics ; Autistic Disorder/genetics ; Biomarkers/metabolism ; Child ; Child, Preschool ; Chromosome Disorders ; Comparative Genomic Hybridization ; Disease Susceptibility ; Female ; Gene Expression Profiling ; Humans ; In Situ Hybridization, Fluorescence ; Infant ; Infant, Newborn ; Male ; Middle Aged ; Oligonucleotide Array Sequence Analysis ; Speech Disorders/genetics ; Young Adult

المؤلفون: Clement CG; Departments of Pathology, University of Texas Medical Branch, Galveston, USA., Potluri VR, Gonzales J, Qian YW

المصدر: International journal of clinical and experimental pathology [Int J Clin Exp Pathol] 2011; Vol. 4 (7), pp. 722-6. Date of Electronic Publication: 2011 Sep 30.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: e-Century Pub. Corp Country of Publication: United States NLM ID: 101480565 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1936-2625 (Electronic) Linking ISSN: 19362625 NLM ISO Abbreviation: Int J Clin Exp Pathol Subsets: MEDLINE

مواضيع طبية MeSH: Chromosomes, Human, Pair 11* , Chromosomes, Human, Pair 5* , Translocation, Genetic*, Conjunctival Neoplasms/*genetics , Lymphoma, B-Cell, Marginal Zone/*genetics, Adult ; Biomarkers, Tumor/analysis ; Conjunctival Neoplasms/chemistry ; Conjunctival Neoplasms/pathology ; Humans ; Immunohistochemistry ; Karyotyping ; Lymphoma, B-Cell, Marginal Zone/chemistry ; Lymphoma, B-Cell, Marginal Zone/pathology ; Male

المؤلفون: Gilbert F; Medical Genetics/Pediatrics, Mount Sinai School of Medicine, New York, NY 10029., Tsao KL, LaLatta F, Xu L, Potluri VR, LaBadie G

المصدر: Progress in clinical and biological research [Prog Clin Biol Res] 1988; Vol. 271, pp. 17-29.

نوع المنشور: Journal Article; Research Support, U.S. Gov't, P.H.S.

بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7605701 Publication Model: Print Cited Medium: Print ISSN: 0361-7742 (Print) Linking ISSN: 03617742 NLM ISO Abbreviation: Prog Clin Biol Res Subsets: MEDLINE

مواضيع طبية MeSH: Disease Models, Animal* , Gene Amplification* , Neoplasm Metastasis* , Oncogenes*, Neuroblastoma/*genetics, Animals ; Cell Line ; Humans ; Karyotyping ; Mice ; Mice, Nude

المؤلفون: Potluri VR, Singh IP, Bhasin MK

المصدر: The Journal of heredity [J Hered] 1987 Jan-Feb; Vol. 78 (1), pp. 55-7.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Oxford University Press For The American Genetic Association Country of Publication: United States NLM ID: 0375373 Publication Model: Print Cited Medium: Print ISSN: 0022-1503 (Print) Linking ISSN: 00221503 NLM ISO Abbreviation: J Hered Subsets: MEDLINE

مواضيع طبية MeSH: Polymorphism, Genetic*, Y Chromosome/*analysis, Fetal Blood/analysis ; Humans ; India ; Infant, Newborn ; Male