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Practical Documents

Some tests require specific documents to be provided with the sample: test request forms, clinical information forms, consent, ... Those documents may be downloaded from the list below:

  References
   
Test request form as interactive PDF for directly typing the information required using
predefined fields in the form.
FDA_BIO


PRENATAL DIAGNOSIS

  References




Cell‐free DNA screening for trisomy 13,18 and 21: test request form
T21FT

Cell‐free DNA screening for trisomy 13,18 and 21: certificate of patient information by the prescribing physician and patient informed consent form
T21FO

Cell‐free DNA screening for trisomy 13,18 and 21: conditions for collecting and sending the sample
T21CD




Preeclampsia Risk assessmentFPECLA

   

Prenatal Diagnosis: analyses request form PRENGB

Consent form for pregnant women requiring in utero diagnosis CONLGB

Fetal Rhesus D genotyping from maternal blood: test request form FRHDGB

Determination of fetal sex from maternal blood: test request form SEXFGB

First or second trimester maternal serum screening combined test DSTFGB

Sampling calendar: Down’s syndrome first or second trimester maternal serum screening CALENDRIER_GB


PROCEDURES FOR PRENATAL DIAGNOSIS References


Procedure for Amniotic fluid collection PROCGB
Procedure for Fetal blood PROSGB
Procedure for Chorionic villus VILCGB


POSTNATAL DIAGNOSIS

INFORMATION FOR GENETIC CHARACTERS INVESTIGATION :

References
   
Genetics testing: informed consent CONSGB
Developmental disorder and genetic diseases: information for genetic characters
FDEMGB
Genetic and pharmacogenetic predisposition INDFGB
A chromosome investigation on DNA chip (CIDC) has been prescribed to you or to your child
ACPAEN
Chromosome investigation on DNA chip: CIDC (CGH-array): Prescription and clinical-pathological informationFCPAEN
Whole exome sequencing -wes
EXOCPT

SOME GENETIC INVESTIGATIONS :

References
   
Familial Mediterranean Fever (analysis MEFV gene): Genetic testing hereditary
auto-inflammatory syndrome
GFMFGB
Genetics study of haemophilia A and B : (analysis F8 gene and F9 gene): resquest form HEABGB
Haemoglobin analysis : (analysis HBB gene, HBA1 gene and HBA2 gene): request form HEMOGB
CFTR gene test: requisition form CFTRGB
Molecular diagnosis of the SHOX gene: request form SHOXGB
Noonan syndrome (PTPN11 gene): request form NOONGB
Rett Syndrome (analysis MECP2 gene): request form RETTGB
Molecular diagnosis of the GJB2 gene (connexin 26) and GJB6 gene (connexin 30) CONNGB
PROCEDURES FOR USE
References


Perchloric acid kit for the determination of pyruvic acid KETONE BODIES CETOEN
Strips for TEARS SAMPLING LARMEN
Transport and conservation medium for UROGENITAL MYCOPLASMA CULTUREMYCOEN
Acetic acid kit for the determination of PHOPHATASE ACID, TOTALEPHOSEN
QUANTIFERON®QUANEN


ALLERGY


References
   
Anaphylactic shock: patient information form CHSAGB

AUTOIMMUNITY


References


Infliximab and anti-infliximab antibodies assay
INFLEN
Adalimumab and anti-adalimumab antibodies assay ADALEN


HAEMATOLOGY


References
   
Cytology-Immunophenotyping: analyses request form HEMTGB
Immuno-haematology: analyses request form AGGLGB
Study of haemoglobin: analyses request formHEMOBI
Glucose transporter deficiency syndrome
GLUT1DS


HEMOSTASIS


References
   
Pre-analytical precautions for hemostasis tests HEMOSTASIS


ONCO-HEMATOLOGY


References
   
Cytogenetics request form HEMAGB


PHARMACOLOGY


References
   
Antiretroviral drugs: Assay ANTIGB
Imatinib (Glivec®): Plasmatic assay IMATGB
Mycophenolate Mofetil (for Cellcept ® only): Pharmacological therapeutic MYCOGB


PATHOLOGY AND CYTOLOGY
  Références
   
Urine smear FROURI_EN
Cervical cytology form EXACYT_EN
Tumoral Genotyping (analysis KRAS gene): request formKRASGB


CANCEROLOGY
  Références
   
Urinary PCA3 test PCA3
Plasmatic detection test for EGFR gene mutationsEGFR