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Short commentaryP:33-34
Human HOXA1 Syndromes Partial chromosome 7 duplication and HOXA1 Gene
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Neuromuscular disorders in children and adolescents
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Recognising the risk of endometriosis using machine learning and Deep Learning techniques
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Genetic predisposition to cancer
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Hepatocyte polarity and plasticity in the wake of hcv infection
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Parkinson's disease and vitamin d
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Neonatologists' perspectives on genetic testing procedures
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Jacob Leo,George Willams
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Short communicationP:7
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GeneticTesting for Hereditary Hemorrhagic Telangiectasia (HHT) ToImprove Patient Management
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CommentaryP:1-1
CommentaryP:1-1
EditorialP:1-1
CommentaryP:1-1
Genetic Medicines: Psychotherapy to Achieve For Hereditary Disorders
EditorialP:1
Basics of Physical and Functional Units of Heredity
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PerspectiveP:1
Assemble DNA Damage Linked to Monogenic in an Infrequent Pediatric Disorder
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2020 Conference Announcement
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Market Analysis Euro Genetic Engineering 2020
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Awards 2020P:1
Juan Castellano
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Genetics and Molecular Biology Webinar 2020
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Awards 2020
Awards @ Nursing Research 2020
Alireza
EditorialP:1
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Shalini Singh
Awards 2020P:1
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Sarantuya JAV
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Sarantuya JAV
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2020 Announcement of 16th International Conference on Surgical Pathology and Cancer Diagnosis
Alexander Birbrair
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A case of Hematometra with a chromosomal abnormality: A case report
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Najafi M *, Rouhi MA, Mokhtari R, Kazemi H
EditorialP:1