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Publications by Blake C Ballif

Corrigendum: A Copy Number Variation Morbidity Map of Developmental Delay

Nature Genetics
Genetics
2014English

Proximal Microdeletions and Microduplications of 1q21.1 Contribute to Variable Abnormal Phenotypes

European Journal of Human Genetics
Genetics
2012English

Delineation of Mechanisms and Regions of Dosage Imbalance in Complex Rearrangements of 1p36 Leads to a Putative Gene for Regulation of Cranial Suture Closure

European Journal of Human Genetics
Genetics
2004English

FISHing for Mechanisms of Cytogenetically Defined Terminal Deletions Using Chromosome-Specific Subtelomeric Probes

European Journal of Human Genetics
Genetics
2000English

Construction of a Natural Panel of 11p11.2 Deletions and Further Delineation of the Critical Region Involved in Potocki–Shaffer Syndrome

European Journal of Human Genetics
Genetics
2005English

Expanding the Clinical Phenotype of the 3q29 Microdeletion Syndrome and Characterization of the Reciprocal Microduplication

Molecular Cytogenetics
BiochemistryMolecular MedicineGeneticsMolecular Biology
2008English

Microdeletion of 6q16.1 Encompassing EPHA7 in a Child With Mild Neurological Abnormalities and Dysmorphic Features: Case Report

Molecular Cytogenetics
BiochemistryMolecular MedicineGeneticsMolecular Biology
2009English

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