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Family Histories sentence examples within Positive Family Histories

Relationships among consanguinity, family history, and the onset of type 1 diabetes in children from Saudi Arabia.

Pallidal degenerations and related disorders: an update

Family Histories sentence examples within Strong Family Histories

Abnormal screens among nonmutation carriers in the High Risk Ontario Breast Screening Program

Prostate-Specific Antigen Screening and Active Surveillance for High-Risk Individuals.

Family Histories sentence examples within Without Family Histories

Stigmatization towards cancer among university students in Malaysia

Association of family history of schizophrenia and clinical outcomes in individuals with eating disorders.

Family Histories sentence examples within Detailed Family Histories

Chorioretinal dystrophy, hypogonadotropic hypogonadism, and cerebellar ataxia: Boucher-Neuhauser syndrome due to a homozygous (c.3524C>G (p.Ser1175Cys)) variant in PNPLA6 gene

Genes and environment in multiple sclerosis: Impact of temporal changes in the sex ratio on recurrence risks.

Family Histories sentence examples within Negative Family Histories

Genetic counseling and testing rates among community cancer programs for patients with breast cancer following site-directed quality improvement.

Towards a Mentoring Model That Enhances Academic, Social, and Cultural Capital in Turbulent Times

Family Histories sentence examples within Extended Family Histories

Justifying inherited wealth: Between ‘the bank of mum and dad’ and the meritocratic ideal

Deflecting Privilege: Class Identity and the Intergenerational Self

Elevated Lipoprotein(a): Background, Current Insights and Future Potential Therapies

Outcomes of retesting in patients with previously uninformative cancer genetics evaluations.

Children Who Perpetrate Family Violence Are Still Children: Understanding and Responding to Adolescent to Parent Violence

Combined effects of cigarette smoking, DNA methyltransferase 3B genetic polymorphism, and DNA damage on lung cancer

Deviations From Standard Family Histories and Subjective Wellbeing at Older Ages

Importance of Family History of Colorectal Cancer In Situ Versus Invasive Colorectal Cancer: A Nationwide Cohort Study.

Family history assessment significantly enhances delivery of precision medicine in the genomics era

A rare mutation in the COLQ gene causing congenital myasthenic syndrome with remarkable improvement to fluoxetine: A case report

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The importance of variants of unknown significance (VUS) in BRCA mutation.

Exploring the outcomes and experiences of Black and White athletes following a sport-related concussion: a retrospective cohort study.

An unusual ECG change after a car crash

Environmental science and pollution research role of heavy metal concentrations and vitamin intake from food in depression: a national cross-sectional study (2009–2017)

Teenagers and Precision Psychiatry: A Window of Opportunity

Experience Completing Population Screening for Variants Associated With Endocrine Tumor Syndromes in a Large, Healthcare-Based Cohort

Correlates of obsessive-compulsive and related disorders symptom severity during the COVID-19 pandemic

Patient and clinician experiences of uncertainty in the diagnostic process: Current understanding and future directions.

Effects of heavy metal, vitamin, and curry consumption on metabolic syndrome during menopause: a Korean community-based cross-sectional study

How memory survives: Descendants of Auschwitz survivors and the progenic tattoo

Fuenzalida de Nona Fernández: reuniendo piezas perdidas

Azai Dosi Kfaang (Modern or Families of Newness): Kom Families from Village to Coast and Further Diasporic Spaces

Advances in Genetic Diagnosis of Kallmann Syndrome and Genetic Interruption

Dermatomyositis following Biosimilar Trastuzumab in a Breast Cancer Patient: A Case Report

Sudden cardiac death due to ARVC in the young: molecular autopsy by whole exome sequencing of DNA from dried blood spots (DBS) collected at birth

A 12-Year-Old Girl Presenting With Recurrent Dyspnea and Pulmonary Ground-Glass Opacities.

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Clinical Characteristics of Pediatric Patients with Congenital Erythrocytosis: A Single Center Study

Genomic, Clinical, and Behavioral Characterization of 15q11.2 BP1-BP2 Deletion (Burnside-Butler) Syndrome in Five Families

Judicious History and Examination Revealing a Rare Diagnosis of Familial Partial Lipodystrophy in a 32-Year-Old Woman With Life-Threatening Pancreatitis due to Hypertriglyceridemia

iPSC-Derived Hereditary Breast Cancer Model Reveals the BRCA1-Deleted Tumor Niche as a New Culprit in Disease Progression

Inferior Rectus Hypoplasia Simulating Contralateral Hypotropia: A Pediatric Case Report

Curvilinear violaceous plaques along Blaschko lines

Clinical Characteristics And Identification of Novel TGF-β1 Mutation In Three Unrelated Chinese Families With Progressive Diaphyseal Dysplasia

Genetic counselor approaches to BRCA1/2 direct‐to‐consumer genetic testing results

Rare cause of high anion gap metabolic acidosis in an infant: Succinyl‐CoA:3‐ketoacid transferase deficiency

Family History in an Old Genre: The Strange Tales of Lü Meisun and Guo Zeyun


Epistaxis Due to Platelet Dysfunction in a Healthy Person During Office Reconstruciton

Legal Oral Histories in Cambridge ESA: Some Examples of Researching Personal, Institutional, and Social Developments

Intraosseous epithelioid haemangioendothelioma of the mandible

The Astronomer and the Witch: Johannes Kepler’s Fight for his Mother

Reflecting on the Past: The Role of Biographical, Familial and Social Memory in New Mothers Interpretations of Emotional Experiences in Early Parenthood

Comparison of Ajmaline and Procainamide Provocation Tests in the Diagnosis of Brugada Syndrome.

Case 2: Fever, Chills, and Abdominal Pain in a 4-year-old Girl

Genetic Data Are a Prerequisite for Interpreting Clinical and Muscle Biopsy Findings in MELAS

Genetic counseling for consumer‐driven whole exome and whole genome sequencing: A commentary on early experiences

High Prevalence of EGFR Mutations in Lung Adenocarcinomas From Brazilian Patients Harboring the TP53 p.R337H Variant.

Famiglie, bambini e insegnanti: verso un’idea integrata di educazione, di benessere e di sviluppo tra contesti

A Relational Approach to Designing Social Technologies that Foster Use of the Kuku Yalanji Language

Isolated abdominal aortic tortuosity diagnosed by fetal echocardiography

Social work and neoliberalism: the Trondheim papers



Findings of metabolic bone disease in infants with unexplained fractures in contested child abuse investigations: a case series of 75 infants

Prevalence of Dyslipidemia in Undiagnosed Palestinian Men: A Cross-Sectional Study

Use of genetic risks in pediatric organ transplantation listing decisions: A national survey

Bilateral Tonic Pupils and Guillain-Barre Syndrome in a 6-Year-Old Boy

Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project.

“Face of the Giant Panda” Sign in Wilson Disease

Mapping women’s knowledges of antiracist teaching in the United States: A feminist phenomenological study of three antiracist women teacher educators

The Haunting Presence of Lost Futures in The Third Reel by S.J. Naudé

The natural history of type B aortic dissection in patients with PRKG1 mutation c.530G>A (p.Arg177Gln).

Phase II trial of GEMOX for the advanced pancreatic cancer with family/personal history of HBOC related cancer

Spontaneous pneumothorax and hemothorax frequently precede the arterial and intestinal complications of vascular Ehlers–Danlos syndrome

Spectrum and clinical relevance of PALB2 germline mutations in 7657 Chinese BRCA1/2-negative breast cancer patients

Self- Reported Personal and Family History of Cancers in Brunei Darussalam: Result of an Integrated Health Survey

Eleven-year follow-up of a Japanese retinitis pigmentosa patient with an HK1 gene mutation

MYH7 Gene-Related Mutation p.V878L Identified in a Chinese Family with Hypertrophic Cardiomyopathy.

Inhibitors among patients with hemophilia in Basra, Iraq – A single center experience

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