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Microdeletion syndrome
Familial Intellectual Disability As a Result of a Derivative Chromosome
3 Chromosome Chapter
Full A-Z List of Genetic Tests Document Reference Number: 413.001
See Shalini C Reshmi's Curriculum Vitae
Cytogenetic Abnormalities in 772 ... -.: Scientific Press International Limited
Deletion 2Q24
Chromosome 17
Aneuploidy and More in Neural Diversity and Disease
In Two Patients with 16P11.2 Microdeletion Syndrome
Verifi Plus Handout
Medical Sciences
Dissecting Molecular Genetic Mechanisms of 1Q21.1 CNV in Neuropsychiatric Disorders
Chromosome 5
Prenatal Diagnosis of Chromosomal Aberrations by Chromosomal
1P36 Deletion Syndrome
Retrospective Karyotype Study in Mentally Retarded Patients
Somatic/Gonadal Mosaicism for Structural Autosomal Rearrangements: Female Predominance Among Carriers of Gonadal Mosaicism for Unbalanced Rearrangements Natalia V
ORPHA Number Disease Or Group of Diseases 300305 11P15.4
Top View
The Presence of Two Rare Genomic Syndromes, 1Q21 Deletion and Xq28 Duplication, Segregating Independently in a Family with Intellectual Disability
9P24 Triplication and 15Q13 Deletion in Syndromic Hydrocephalus with Diffuse Villous Hyperplasia of the Choroid Plexus
About the Prenatalsafe® Prenatal Test the Prenatalsafe® Non-Invasive Prenatal Test (NIPT) Looks at the DNA (Genetic Material) in Your Blood
Prenatal Detection of Unbalanced Chromosomal Rearrangements by Array-CGH
7Q35 Microdeletion and 15Q13.3 and Xp22.33 Microduplications in A
Proximal Microdeletions and Microduplications of 1Q21.1 Contribute to Variable Abnormal Phenotypes
2Q23.1 Microdeletion Syndrome
15Q13.3 Microdeletion
The 15Q11.2 BP1-BP2 Microdeletion
15Q Deletions FTNW
Non-Invasive Prenatal Aneuploidies and Microdeletion Screening Test Report
The Genetics of Microdeletion and Microduplication Syndromes: an Update
Type 1 Established Condition List
Chromosomal Basis of Human Diseases
The Discovery of Microdeletion Syndromes in the Post-Genomic Era: Review of the Methodology and Characterization of a New 1Q41q42 Microdeletion Syndrome Lisa G
Consequences of 22Q11.2 Microdeletion on the Genome, Individual and Population Levels
Identification of Genomic Loci Contributing to Agenesis of the Corpus Callosum Mary C
Chromosome 15
Chromosome 15Q24 Microdeletion Syndrome Pilar L Magoulas1 and Ayman W El-Hattab2*
Nasal Speech and Hypothyroidism Are Common Hallmarks of 12Q15 Microdeletions
Koolen-De Vries Syndrome
Clinical Experience with Multiplex Ligation
Detection for Microdeletion Syndromes in 427 Thai Patients
Deletion and Duplication of 15Q24: Molecular Mechanisms and Potential Modification by Additional Copy Number Variants Ayman W
Medical Genetics and Clinical Applications (With International Participation) 11-13 February, 2016, Kayseri, Turkey