Blood tests and health screening

Genetic

We hope that you find our comprehensive range of genetic blood tests and screens to be of use. Please do not hesitate to contact us should you not be able to locate a specific blood test or health screen.

For all company health screening, occupational health checks and pre-emplyment tests, please visit MediChecks.com's Corporate Health Screening site or call us for further information on how we can benefit your organisation.

Genetic
  22q11 Deletion  
  Achondroplasia  
  Alpha 1 Antitrypsin Genotype  
  Alpha Feto Protein on Amniotic fluid  
  Amnio PCR only  
  Amniocentesis Culture  
  Androgen Insensitivity  
  Angelman syndrome - UPD 15  
  Angelmann's syndrome  
  Angelmann's syndrome karyotype / FISH  
  Angelmann's Syndrome Sequencing UBE3A  
  Ashkenasi Jewish Screen  
  Becker Muscular Dystrophy  
  Bloom Syndrome  
  BRCA1 / BRCA2  
  Breast Cancer  
  CADASIL  
  Canavans Disease  
  Chromosome Analysis  
  Chromosome Analysis  
  Chromosome Analysis  
  Chromosome Analysis  
  Chromosome Analysis (Culture)  
  Chromosome Analysis (PCR and Culture)  
  Chromosome with Fragile X  
  Chromosome Y Deletion  
  Chronic Granulomatous Disease - Primary Screen  
  Congenital absence of vas deferens (CF and polyT (5T) and Y deletions)  
  Connexin 26  
  Cowden syndrome  
  Cri du Chat karyotype / FISH  
  Cystic Fibrosis  
  Cystic Fibrosis (7 Ashkenazi Jewish mutations)  
  Deafness - aminoglycoside induced, mitochondrial / A155G  
  Deafness - Pendred syndrome  
  Deafness (Connexin 26 full screen)  
  Deep Vein Thrombosis Risk Assessment  
  Di George Syndrome  
  Downs Syndrome Confirmation  
  Duchenne Muscular Dystrophy (male/female common deletions and duplications)  
  Duchenne Muscular Dystrophy (mutation analysis)  
  DVT Screen  
  Ectrodactyly-ED-Clefting  
  Erythrokeratoderma variabilis  
  Fabry Disease  
  Factor II Prothrombin gene (G20210A)  
  Factor V Leiden  
  Factor VIII (detection in relative)  
  Factor VIII (new patient)  
  Factor VIII Assay  
  Familial Cutaneous Malignant Melanoma CDKN2A  
  Familial Hibernian Fever  
  Familial Mediterranean Fever (known)  
  Familial Mediterranean Fever (unknown)  
  Fanconi's Anaemia  
  Fragile X Karyotype  
  Freidrich's Ataxia  
  Gaucher Disease  
  Genetic Reporoductive Profile  
  Gorlin syndrome  
  Haemochromatosis  
  Haemophilia B (full mutation screen)  
  Hay-Wells  
  Hereditary Angioedema (known)  
  Hereditary Angioedema (unknown)  
  Hereditary Liability to Pressure Palsy  
  HLA B27  
  HLA Tissue Type A, B, Cw, DRB1, DQB1  
  HLA Tissue Typing A  
  HLA Tissue Typing A, B  
  HLA Tissue Typing B  
  HLA Tissue Typing B27  
  HLA Tissue Typing DR/DQ  
  HLA Tissue Typing Narcolepsy  
  Holoprosencephaly Panel  
  Human Parvovirus B19 DNA  
  Huntingtons Disease  
  Hyper-lgD syndrome  
  Incontinentia Pigmenti  
  Jervell, Lange-Nielsen Syndrome  
  Kennedy Disease  
  Leber's Optic Atrophy  
  Long QT Syndrome Panel  
  Marfan Syndrome  
  MCAD Deficiency  
  Miller Dieker Syndrome  
  Mitochondrial Myopathy  
  MTHFR Variant  
  Multiple Endocrine Nepoplasia type 2B  
  Multiple Epiphyseal Dysplasia  
  Mycoplasma PCR  
  Myotonic Dystrophy  
  Narcolepsy  
  Noonan Syndrome (PTPNII whole gene)  
  Oculopharyngeal Muscular Dystrophy  
  Parvovirus B19 DNA  
  Paternity Test  
  Periodic Fever Syndromes  
  Peutz-Jeghers Syndrome  
  Poly T  
  Post-Natal Paternity Test  
  Prader Willi Syndrome karyotype and FISH  
  Prader Willi Syndrome M-PCR  
  Prader-Willi - UPD 15  
  Pre-Travel Screen  
  Pseudoachondroplasia  
  Recurrent Miscarriage Profile  
  Reilly Day Syndrome  
  Rett syndrome  
  Rubella Virus DNA  
  Rubella Virus PCR  
  Sickle Cell Disease  
  Smith Magennis Syndrome  
  Sotos Syndrome  
  Spinal Muscular Atrophy  
  SRY Gene  
  Tay Sachs Screen  
  Telomeric Screen  
  Thrombotic Risk Profile  
  Trisomy Analysis  
  Uni Parental Disomy  
  Vohwinkel Syndrome  
  Werdnig-Hoffman Disease  
  Williams Syndrome karyotype / FISH  
  Wilms Tumour- WT1/ DDS  
  Wolf Hirschorn Syndrome karyotype / FISH  
  X-linked Hydrocephalus / MASA / (L1CAM)  
  X-linked Hypohidrotic ED (EDA1)  
  Y Chromosome Deletion  
  Zygosity testing (comparative DNA profile)  

Regular health checks together with lifestyle and medical advice for healthy living often provides peace of mind and could help prevent the development of serious illnesses and diseases.

Have control of your future health and well-being!


Please ensure that you understand and agree to our Terms and Conditions before ordering any of the blood tests and health screening services provided by MediChecks.com. For instructions on how to order any of the any of the blood tests and health screening services on-line click here Ordering Process or if you wish to place an order for a any of the blood test and health screen over the telephone please call 08456 029 029 (UK only). Purchases made from outside the UK can be made on +44 115 9890044.

Blood tests and other laboratory tests are done to help make a medical diagnosis. Blood testing is one of the key steps in making a medical diagnosis. Laboratory tests including blood tests can have false positives and false negatives. Interpretation of blood tests takes knowledge of the underlying disease process and experience. The blood tests, services and information on this site are not intended in any way to substitute a medical consultation with your own Doctor.

 
 

Empty!
 
Individual Health Checks
Well-Person.Check
Well-Person.Check PLUS

Well-Man.Check
Well-Man.Check PLUS

Well-Woman.Check
Well-Woman.Check PLUS
 
New
Asprin Allergy
Beryllium Sensitivity
Biotin
BRCA1 / BRCA2
Chlamydia & Gonorrhoea
Chlamydia Trachomatis PCR
Clostridium Difficile Toxin
Coenzyme Q10
Gonorrhoea & Chlamydia
Hair Drug Test
Hair Mineral Analysis
Metabolic Acid Profile
Metal Hypersensitivity Profile 4
PCA3
Polycystic Ovary Syndrome Profile 2
Pre-Operative Screen 3
Salicylates IgE
Sexually Transmitted Diseases
Toxic Metal Screen
Volatile Organic Compound Screen