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Multi-Omics Analysis of SOX4, SOX11, and SOX12 Expression and the Associated Pathways in Human Cancers

Comparative transcriptomes and genome-wide identification reveal salt stress-responsive PP2C in Jute (Corchorus capsularis)

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Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy

Homozygosity mapping and whole exome sequencing reveal a novel ERCC8 mutation in a Chinese consanguineous family with unique cerebellar ataxia.

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The complete chloroplast genome of the Jerusalem artichoke (Helianthus tuberosus L.) and an adaptive evolutionary analysis of the ycf2 gene

The complete chloroplast genome of the Jerusalem artichoke (Helianthus tuberosus L.) and an adaptive evolutionary analysis of the ycf2 gene

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Drug-Induced Liver Injury in a Patient with Nonsmall Cell Lung Cancer after the Self-Administration of Fenbendazole Based on Social Media Information

ITPR1 Mutation Contributes to Hemifacial Microsomia Spectrum

Loperamide-induced cardiotoxicity: a case overlooked?

Targeted next generation sequencing and family survey enable correct genetic diagnosis in CRX associated macular dystrophy – a case report

Lessons from recent medical history: an obsolete anti-reflux device in an older patient with variable gastrointestinal symptoms.

An interbacterial DNA deaminase toxin directly mutagenizes surviving target populations

SOD1-related ALS with anticipation in a large family from Martinique.

ASH1L mutation caused seizures and intellectual disability in twin sisters

Molecular cytogenetic characterization of a de novo chromosome 1q41-q42.11 microdeletion of paternal origin in a 15-year-old boy with mental retardation, developmental delay, autism and congenital heart defects.

Severe Early‐Onset Parkinsonian Syndrome Caused by PLA2G6 Heterozygous Variants

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Абиотрофия сетчатки при митохондриальной патологии. NARP-синдром (описание клинического случая)

Genetic Diversity of Seed Storage Protein in Selected Melastomataceae and Fagaceae from Tasik Kenyir

A Novel X-Linked Variant of IQSEC2 is Associated with Lennox-Gastaut Syndrome and Mild Intellectual Disability in Three Generations of a Korean Family.

First family case of haemoglobinopathy Titusville in France and literature overview

SUN-612 Pleural Effusions Revealing Anaplastic Dedifferentiation of Papillary Thyroid Carcinoma

Intestinal myiasis in a very elderly patient with inappropriate home care

Giant Congenital Melanocytic Nevus of Scalp: A Rare Case with Dermoscopic Findings

The Relationship Between Children Education in the Family and Car Driving and Motorcycle Riding Behaviour in Indonesia

Genome-wide mining of respiratory burst homologs and its expression in response to biotic and abiotic stresses in Triticum aestivum

A universal reporter cell line for bioactivity evaluation of engineered cytokine products

Do the nodules detected in chest X‐rays always indicate a disease of lung parenchyma?

Familial deep cavitating state with a glutathione metabolism defect

SUN-545 A Rare Case of Resistance to Thyroid Hormone Due to Novel Mutation in THRB Gene Mistreated as Hyperthyroidism

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Family Revealed 가족 공개

Family Revealed 가족 공개
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