Dkc1 mutation carriers. Medical search. Frequent questions

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Anatomy11

Telomere Fallopian Tubes Cell Line Chromosomes, Human, Pair 6 Brain Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 17 COS Cells Chromosomes, Human, Pair 19 X Chromosome Cells, Cultured

Organisms2

Escherichia coli Saccharomyces cerevisiae

Diseases41

Dyskeratosis Congenita Genetic Predisposition to Disease Breast Neoplasms Ovarian Neoplasms Colorectal Neoplasms, Hereditary Nonpolyposis Hereditary Breast and Ovarian Cancer Syndrome Fallopian Tube Neoplasms Neoplastic Syndromes, Hereditary Romano-Ward Syndrome Cardiomyopathy, Hypertrophic, Familial Breast Neoplasms, Male Paraganglioma Li-Fraumeni Syndrome Syndrome Dystonia Cardiomyopathy, Hypertrophic Long QT Syndrome Colorectal Neoplasms Microsatellite Instability Parkinson Disease Endometrial Neoplasms Dystonic Disorders Optic Atrophy, Hereditary, Leber Neoplasms Gaucher Disease Alzheimer Disease Frontotemporal Lobar Degeneration Adenomatous Polyposis Coli Cystadenocarcinoma, Serous Olfaction Disorders Neoplasms, Second Primary Arrhythmogenic Right Ventricular Dysplasia Genetic Diseases, X-Linked Disease Progression Motor Neuron Disease Melanoma Neoplasms, Multiple Primary Retinitis Pigmentosa Cardiomyopathy, Dilated Peritoneal Neoplasms Pheochromocytoma

Chemicals and Drugs59

BRCA2 Protein BRCA1 Protein Nuclear Proteins Telomerase Cell Cycle Proteins RNA, Ribosomal, 28S Carrier Proteins MutS Homolog 2 Protein Drug Carriers Codon, Nonsense DNA-Binding Proteins Acyl Carrier Protein Transcription Factors Glucosylceramidase Neoplasm Proteins DNA Primers Adaptor Proteins, Signal Transducing Presenilin-1 DNA, Neoplasm Reduced Folate Carrier Protein Membrane Proteins DNA Plakophilins NAV1.5 Voltage-Gated Sodium Channel Codon Tumor Suppressor Protein p53 Tumor Suppressor Proteins DNA Repair Enzymes Bacterial Proteins Proto-Oncogene Proteins Protein-Serine-Threonine Kinases Genetic Markers RNA, Messenger Mutant Proteins Bone Morphogenetic Protein Receptors, Type II Succinate Dehydrogenase KCNQ1 Potassium Channel Membrane Transport Proteins Cardiac Myosins DNA, Mitochondrial Lamin Type A Recombinant Proteins Adenosine Triphosphatases Ubiquitin-Protein Ligases Proto-Oncogene Proteins B-raf Contraceptives, Oral Rad51 Recombinase DNA Glycosylases Sodium Channels Phthalazines Proteins Nuclear Receptor Coactivator 3 Saccharomyces cerevisiae Proteins Recombinant Fusion Proteins Nerve Tissue Proteins Eye Proteins Trans-Activators Escherichia coli Proteins Receptors, Estrogen

Analytical, Diagnostic and Therapeutic Techniques and Equipment48

Heterozygote Detection Pedigree Genetic Testing DNA Mutational Analysis Salpingectomy Polymerase Chain Reaction Amino Acid Substitution Case-Control Studies Drug Carriers Ovariectomy Risk Factors Sequence Analysis, DNA Mutagenesis, Site-Directed Mastectomy Genetic Association Studies Risk Risk Assessment Cohort Studies Models, Molecular Chromosome Mapping Models, Genetic Cloning, Molecular Genetic Complementation Test Immunohistochemistry Magnetic Resonance Imaging Incidence Mammography Sequence Alignment Prognosis Transfection Registries Retrospective Studies Sterilization, Tubal Salpingostomy Mutagenesis, Insertional Reverse Transcriptase Polymerase Chain Reaction Therapeutic Irrigation Odds Ratio Sensitivity and Specificity Early Diagnosis Prevalence Abortion, Therapeutic Follow-Up Studies Kaplan-Meier Estimate Magnetic Resonance Imaging, Cine Genome-Wide Association Study Proportional Hazards Models Crosses, Genetic

Psychiatry and Psychology3

Family Alzheimer Disease Frontotemporal Lobar Degeneration

Phenomena and Processes89

Genes, BRCA1 Heterozygote Mutation Genes, BRCA2 Germ-Line Mutation Point Mutation Mutation, Missense Genetic Predisposition to Disease Penetrance Frameshift Mutation Founder Effect Genotype Phenotype Alleles DNA Mismatch Repair Exons Base Sequence Amino Acid Substitution Telomere Polymorphism, Single-Stranded Conformational Mutation Rate Homozygote Polymorphism, Single Nucleotide Polymorphism, Genetic Codon, Nonsense Amino Acid Sequence Gene Frequency Sequence Deletion Genes, Dominant Gene Deletion Risk Mutagenesis Genes, p53 Genes, Recessive Genetic Linkage Microsatellite Repeats Genetic Variation Protein Structure, Tertiary Suppression, Genetic Binding Sites Sequence Homology, Amino Acid Codon Base Pair Mismatch Loss of Heterozygosity Microsatellite Instability Protein Binding Promoter Regions, Genetic Haploinsufficiency DNA Repair Haplotypes Genetic Markers Plasmids Kinetics Genetic Heterogeneity Consanguinity Transfection Genes, p16 Time Factors Protein Conformation Genes, Lethal Genes, APC Transcription, Genetic Mutagenesis, Insertional Exome Chromosomes, Human, Pair 6 Introns Gene Expression Genes, Bacterial Structure-Activity Relationship Epistasis, Genetic Polymorphism, Restriction Fragment Length Chromosomes, Human, Pair 9 Odds Ratio Gene Expression Regulation, Neoplastic Recombination, Genetic Genes, Tumor Suppressor Genes Sensitivity and Specificity Temperature Chromosomes, Human, Pair 17 Biological Transport Signal Transduction Drug Resistance, Viral Conserved Sequence Genes, Suppressor Chromosomes, Human, Pair 19 X Chromosome INDEL Mutation Protein Structure, Secondary

Disciplines and Occupations2

Genetic Counseling Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena1

Information Science6

Base Sequence Molecular Sequence Data Amino Acid Sequence Incidence Registries Prevalence

Named Groups2

Jews Asian Continental Ancestry Group

Health Care22

Genetic Testing Carrier State Family Health Age of Onset Genetic Counseling Case-Control Studies Risk Factors Risk Risk Assessment Cohort Studies Age Factors Incidence Registries Retrospective Studies Odds Ratio Sensitivity and Specificity Temperature Prevalence Follow-Up Studies Kaplan-Meier Estimate Genome-Wide Association Study Proportional Hazards Models

Geographicals10

Iceland Australia Israel Canada North America France Europe District of Columbia Netherlands Italy

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Information Science Named Groups Health Care Geographicals

Dyskeratosis Congenita Genes, BRCA1 Heterozygote Mutation Genes, BRCA2 Germ-Line Mutation Point Mutation Mutation, Missense BRCA2 Protein Heterozygote Detection BRCA1 Protein Pedigree Genetic Predisposition to Disease Genetic Testing Nuclear Proteins Penetrance Telomerase Breast Neoplasms Frameshift Mutation Jews DNA Mutational Analysis Cell Cycle Proteins Salpingectomy Founder Effect Ovarian Neoplasms Genotype Carrier State Colorectal Neoplasms, Hereditary Nonpolyposis RNA, Ribosomal, 28S Family Health Age of Onset Phenotype Alleles Hereditary Breast and Ovarian Cancer Syndrome Carrier Proteins DNA Mismatch Repair Genetic Counseling Fallopian Tube Neoplasms Exons MutS Homolog 2 Protein Polymerase Chain Reaction Base Sequence Amino Acid Substitution Telomere Case-Control Studies Molecular Sequence Data Polymorphism, Single-Stranded Conformational Mutation Rate Homozygote Drug Carriers Neoplastic Syndromes, Hereditary Polymorphism, Single Nucleotide Ovariectomy Risk Factors Polymorphism, Genetic Romano-Ward Syndrome Codon, Nonsense Amino Acid Sequence Gene Frequency DNA-Binding Proteins Cardiomyopathy, Hypertrophic, Familial Sequence Analysis, DNA Sequence Deletion Genes, Dominant Mutagenesis, Site-Directed Acyl Carrier Protein Mastectomy Genetic Association Studies Transcription Factors Family Gene Deletion Risk Glucosylceramidase Mutagenesis Risk Assessment Genes, p53 Cohort Studies Neoplasm Proteins Genes, Recessive Breast Neoplasms, Male DNA Primers Adaptor Proteins, Signal Transducing Paraganglioma Li-Fraumeni Syndrome Genetic Linkage Escherichia coli Presenilin-1 Fallopian Tubes Microsatellite Repeats Syndrome DNA, Neoplasm Genetic Variation Reduced Folate Carrier Protein Dystonia Protein Structure, Tertiary Membrane Proteins DNA Cardiomyopathy, Hypertrophic Models, Molecular Long QT Syndrome

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