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- Fusion Genes and Rnas in Cancer Development
- Monosomy 22 with Mosaicism References SUMMARY a 2-Year-Old Male Child with Mosai- Rethore MO, Couturier J, Carpentier S, Ferrand J, Lejeune J
- Phelan-Mcdermid Syndrome (22Q13 Deletions)
- Retrospective Karyotype Study in Mentally Retarded Patients
- Prospective Study of Autism Phenomenology and The
- A Common Cause for Phelan-Mcdermid Syndrome and Neurofibromatosis Type 2: One Ring to Bind Them Ariel M
- Somatic/Gonadal Mosaicism for Structural Autosomal Rearrangements: Female Predominance Among Carriers of Gonadal Mosaicism for Unbalanced Rearrangements Natalia V
- Cytogenetic Findings in Patients with Intellectual Disability/Mental Retardation and Dysmorphic Features in Eastern Croatia 1
- Etiological Heterogeneity in Autism Spectrum Disorders: More Than 100 Genetic and Genomic Disorders and Still Counting
- Forty-Two Supernumerary Marker Chromosomes (Smcs) in 43 273 Prenatal Samples: Chromosomal Distribution, Clinical Findings, and UPD Studies
- Williams-Beuren Syndrome: Phenotypic Variability and Deletions of Chromosomes 7, 1 1, J Med Genet: First Published As 10.1136/Jmg.33.12.986 on 1 December 1996
- Prof. OSMAN DEMİRHAN Personal Information Efmaxa Ipl:H Osndee:M +Ir9@0 C3u2.E2d 3U3.T8r 7140 Awdedbr:E Hstst:P Sç:U/K/Uavroesvias .Ücun.E
- Research Progress of Chimeric RNA and Health
- Inheritance of a Ring 14 Chromosome
- Fusion Transcripts of Adjacent Genes: New Insights Into the World of Human Complex Transcripts in Cancer
- Prof.Dr. OSMAN DEMİRHAN Kişisel Bilgiler EF-Apxo Tsetale: Foosndue:M +Ir9@0C 3U2.E2d U3.3Tr8 7140 Pwoesbta: Hatdtprse:/S/I:A Vçeuskius.Rcouv.Ead Üu.Ntr
- Chromosomal Anomalies and the Eye J
- Ring 22 FTNW
- Neuropsychiatric Decompensation in Adolescents and Adults with Phelan
- Phelan-Mcdermid Syndrome: a Review of the Literature and Practice
- Ring 22 Duplication/Deletion Mosaicism: Clinical, Cytogenetic, and Molecular Characterisation J Med Genet: First Published As 10.1136/Jmg.36.3.237 on 1 March 1999
- Therapeutic and Diagnostic Agents
- Complex Biology of Constitutional Ring Chromosomes Structure and (In)Stability Revealed by Somatic Cell Reprogramming T
- A Marfan Syndrome-Like Phenotype Caused by a Neocentromeric Supernumerary Ring Chromosome 15 Shane C
- Molecular Characterisation of a Ring Chromosome 22 in a Patient with Severe Language Delay: a Contribution to the Refinement Of
- 3Disease Browser: a Web Server for Integrating 3D Genome and Disease
- Atypical Teratoid Rhabdoid Brain Tumor in an Infant with Ring Chromosome 22
- Ring Chromosomes in Human Neoplasias
- 51337207.Pdf
- 22 Chromosome Chapter
- Prevalence and Incidence of Rare Diseases: Bibliographic Data
- Kb Triplication in the Cat Eye Syndrome Critical Region Causes Anorectal, Renal and Preauricular Anomalies in a Three-Generation Family
- Prevalence and Incidence of Rare Diseases
- Coexistence of Autism and Ring Chromosome 22
- Points of View
- RING CHROMOSOME 22: a REVIEW of the LITERATURE and FIRST REPORT from INDIA Mahajan S1, Kaur A2,*, Singh JR3
- Human Ring Chromosome Registry for Cases In
- Patient Organizations in Connection with Small Supernumerary Marker Chromosomes
- 22Q13.2Q13.32 Genomic Regions Associated with Severity of Speech Delay, Developmental Delay, and Physical Features in Phelan–Mcdermid Syndrome