Bloom s syndrome phenotype. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy8

Chromosomes, Human, Pair 21 Cells, Cultured Cell Line Fibroblasts Chromosomes, Human, Pair 15 Brain Chromosomes, Human, Pair 22 Skin

Organisms25

Phytoplankton Microcystis Dinoflagellida Diatoms Nodularia Haptophyta Stramenopiles Cyanobacteria Zooplankton Porcine respiratory and reproductive syndrome virus Chrysophyta Aphanizomenon Mice, Inbred C57BL Eukaryota Mice, Knockout Microalgae Cylindrospermopsis Scyphozoa Mice, Transgenic Plankton Mice, Mutant Strains Saccharomyces cerevisiae Roseobacter Ctenophora Alphaproteobacteria

Diseases101

Syndrome Upper Extremity Deformities, Congenital Down Syndrome Abnormalities, Multiple Antley-Bixler Syndrome Phenotype Limb Deformities, Congenital Trisomy Intellectual Disability Chromosome Deletion Disease Models, Animal Metabolic Syndrome X Telangiectasis Nephrotic Syndrome Werner Syndrome Sjogren's Syndrome Turner Syndrome Facial Dermatoses Myelodysplastic Syndromes Dwarfism Shellfish Poisoning Cushing Syndrome Polycystic Ovary Syndrome Williams Syndrome Acute Coronary Syndrome DiGeorge Syndrome Prader-Willi Syndrome Long QT Syndrome Horner Syndrome Guillain-Barre Syndrome Hemolytic-Uremic Syndrome Tourette Syndrome Compartment Syndromes Antiphospholipid Syndrome Bloom Syndrome Klinefelter Syndrome Porcine Reproductive and Respiratory Syndrome Bartter Syndrome Carpal Tunnel Syndrome Reye Syndrome Angelman Syndrome Ehlers-Danlos Syndrome Brugada Syndrome HELLP Syndrome Respiratory Distress Syndrome, Adult Rothmund-Thomson Syndrome Facies Wiskott-Aldrich Syndrome Job Syndrome Severe Acute Respiratory Syndrome Restless Legs Syndrome Craniofacial Abnormalities Acquired Immunodeficiency Syndrome Paraneoplastic Syndromes Sweet Syndrome Eye Abnormalities Kallmann Syndrome Churg-Strauss Syndrome Sturge-Weber Syndrome Genetic Predisposition to Disease Chediak-Higashi Syndrome Photosensitivity Disorders Budd-Chiari Syndrome Bardet-Biedl Syndrome Usher Syndromes Sezary Syndrome Wolff-Parkinson-White Syndrome Sick Sinus Syndrome Beckwith-Wiedemann Syndrome Alagille Syndrome Felty Syndrome Stevens-Johnson Syndrome Cockayne Syndrome Chromosome Aberrations Immunologic Deficiency Syndromes Oculocerebrorenal Syndrome Peutz-Jeghers Syndrome Smith-Lemli-Opitz Syndrome Hand Deformities, Congenital ACTH Syndrome, Ectopic Stiff-Person Syndrome Chromosome Disorders Hemorrhagic Fever with Renal Syndrome Orofaciodigital Syndromes Behcet Syndrome Short Bowel Syndrome Duane Retraction Syndrome Zollinger-Ellison Syndrome Serotonin Syndrome Hepatopulmonary Syndrome Costello Syndrome Syndactyly Proteus Syndrome Hermanski-Pudlak Syndrome Microcephaly Genomic Instability Fanconi Anemia Complex Regional Pain Syndromes Li-Fraumeni Syndrome LEOPARD Syndrome Goldenhar Syndrome Respiratory Distress Syndrome, Newborn

Chemicals and Drugs26

Microcystins Marine Toxins DNA Helicases Oxocins Adenosine Triphosphatases Saxitoxin DNA-Binding Proteins RNA, Messenger Sulfonium Compounds DNA Transcription Factors Nuclear Proteins DNA Primers Exodeoxyribonucleases Phycocyanin Biological Markers Membrane Proteins DNA Topoisomerases, Type I Wiskott-Aldrich Syndrome Protein Carrier Proteins Bacterial Proteins DNA, Bacterial Chlorophyll Genetic Markers DNA, Cruciform Saccharomyces cerevisiae Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment30

Karyotyping In Situ Hybridization, Fluorescence Pedigree Chromosome Mapping Disease Models, Animal Sequence Analysis, DNA DNA Mutational Analysis Polymerase Chain Reaction Facies Genetic Complementation Test Risk Factors Models, Biological Models, Genetic Case-Control Studies Treatment Outcome Cloning, Molecular Immunohistochemistry Reverse Transcriptase Polymerase Chain Reaction Immunophenotyping Crosses, Genetic Blotting, Western Gene Expression Profiling Flow Cytometry Fatal Outcome Retrospective Studies Sequence Alignment Genetic Testing Transfection Prevalence Follow-Up Studies

Psychiatry and Psychology3

Intellectual Disability Tourette Syndrome Restless Legs Syndrome

Phenomena and Processes63

Phenotype Chromosomes, Human, Pair 21 Harmful Algal Bloom Trisomy Eutrophication Chromosome Deletion Mutation Genotype Lakes Seawater Sister Chromatid Exchange Base Sequence Fresh Water Amino Acid Sequence Alleles Heterozygote Oceans and Seas Homozygote Time Factors Gene Deletion Water Movements Mutation, Missense Wind Recombination, Genetic Cell Differentiation Phylogeny Signal Transduction Seasons Genetic Linkage Ecosystem Genetic Variation Consanguinity Genes, Recessive DNA Repair Genetic Predisposition to Disease Biomass Genes, Dominant Pregnancy Gene Expression Regulation Sequence Homology, Amino Acid Chromosomes, Human, Pair 15 Gene Expression Temperature Gene Expression Regulation, Developmental Chromosome Aberrations Point Mutation Food Chain Exons Cell Division DNA Replication Polymorphism, Single Nucleotide Polymorphism, Genetic Species Specificity Sequence Deletion Chromosomes, Human, Pair 22 Protein Structure, Tertiary Mosaicism Genetic Markers Genomic Instability DNA, Cruciform Protein Binding Transfection Cell Proliferation

Disciplines and Occupations3

Water Microbiology Immunohistochemistry Oceanography

Technology, Industry, Agriculture2

Spacecraft Shellfish

Information Science6

Molecular Sequence Data Base Sequence Amino Acid Sequence Phylogeny Fatal Outcome Prevalence

Named Groups1

Infant, Newborn

Health Care20

Lakes Seawater Fresh Water Water Microbiology Water Movements Wind Seasons Ecosystem Risk Factors Environmental Monitoring Biomass Case-Control Studies Treatment Outcome Temperature Food Chain Fatal Outcome Retrospective Studies Genetic Testing Prevalence Follow-Up Studies

Geographicals5

Great Lakes Region Oceans and Seas Atlantic Ocean Pacific Ocean North Sea

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Technology, Industry, Agriculture Information Science Named Groups Health Care Geographicals

Phenotype Syndrome Chromosomes, Human, Pair 21 Upper Extremity Deformities, Congenital Down Syndrome Abnormalities, Multiple Antley-Bixler Syndrome Phenotype Harmful Algal Bloom Limb Deformities, Congenital Trisomy Eutrophication Karyotyping Intellectual Disability Chromosome Deletion In Situ Hybridization, Fluorescence Pedigree Mutation Chromosome Mapping Phytoplankton Genotype Disease Models, Animal Microcystis Metabolic Syndrome X Microcystins Marine Toxins Dinoflagellida Telangiectasis Nephrotic Syndrome Werner Syndrome Sjogren's Syndrome Lakes Molecular Sequence Data DNA Helicases Turner Syndrome Facial Dermatoses Oxocins Seawater Myelodysplastic Syndromes Diatoms Dwarfism Nodularia Shellfish Poisoning Sister Chromatid Exchange Base Sequence Cushing Syndrome Fresh Water Polycystic Ovary Syndrome Haptophyta Williams Syndrome Acute Coronary Syndrome Adenosine Triphosphatases Stramenopiles DiGeorge Syndrome Prader-Willi Syndrome Long QT Syndrome Cyanobacteria Amino Acid Sequence Horner Syndrome Alleles Guillain-Barre Syndrome Hemolytic-Uremic Syndrome Zooplankton Water Microbiology Tourette Syndrome Compartment Syndromes Great Lakes Region Antiphospholipid Syndrome Bloom Syndrome Heterozygote Klinefelter Syndrome Oceans and Seas Cells, Cultured Porcine Reproductive and Respiratory Syndrome Sequence Analysis, DNA DNA Mutational Analysis Bartter Syndrome Homozygote Cell Line Saxitoxin Time Factors Gene Deletion Carpal Tunnel Syndrome Reye Syndrome Polymerase Chain Reaction Water Movements Porcine respiratory and reproductive syndrome virus Chrysophyta Angelman Syndrome Ehlers-Danlos Syndrome Brugada Syndrome Aphanizomenon HELLP Syndrome Mice, Inbred C57BL Mutation, Missense Eukaryota Wind Mice, Knockout Respiratory Distress Syndrome, Adult Microalgae DNA-Binding Proteins

No FAQ available that match "bloom s syndrome phenotype"