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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.

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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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10.1200/JCO.2021.39.15_SUPPL.E22507

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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10.22541/AU.161825363.37305254/V1

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



BLOOD THICKER THAN WATER? STEPGAP IN INTERGENERATIONAL RELATIONSHIPS



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



GEN-03 GENOTYPE-PHENOTYPE CORRELATION IN 111 FAMILIES OF VON HIPPEL-LINDAU DISEASE IN JAPAN



AN ARTS-BASED CURRICULUM ENCOUNTER: WHAT DOES IT MEAN TO LIVE ON THIS LAND?



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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