Prenatal Microarray Requisition Form

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Acct # _________________________________________________
Last Name: _____________________________________________
First Name: _____________________________________________
DOB: ______________________(DD/MM/YYY) Sex: ___________
Healthcard #: _______________________________ VC: _________
PRENATAL MICROARRAY REQUISITION
Address: ________________________________________________
________________________________________________________
GENETICS LABORATORY
2200 Eglinton Ave. W., Rm 2H144
Tel: (905) 813-1100 x6288
Primary Phone #: _________________________________________
Mississauga, ON L5M 2N1 Canada
Fax: (905) 813-3854
Unit # __________________________________________________
To ensure there is no delay in reporting results; please ensure the following accompany each sample:
Completed requisition form
Parental samples. Mother’s sample is mandatory for MCC studies. Father’s sample is highly recommended
(Complete a Separate Prenatal Microarray Requisition for each parent)
PHYSICIAN INFORMATION
Referring Dr: ______________________________________
Copy To:_________________________________________
Registration #:_____________________________________
Registration #:_____________________________________
Address: _________________________________________
Address:_________________________________________
Telephone:__________________ Fax:__________________
Telephone:__________________ Fax:_________________
Signature (required): ________________________________
CLINICAL INFORMATION
SPECIMEN TYPE
Gestation at collection date: ________________weeks
Direct CVS (10-15 mg cleaned villi)
Karyotype result (if known) : __________________________
Cultured CVS (1 T75 or 2 T25 flasks 70% confluent)
Sex of Fetus (if known): ______________
Direct Amniotic Fluid (15cc)
(by
QF-PCR
or
FISH )
Father’s name: ____________________ DOB: ___________
Cultured Amniocytes (1 T75 or 2 T25 flasks 70% confluent)
Please attach pedigree if relevant
DNA: 2ug total (at a minimum concentration of 70 ng/uL)
INDICATION FOR TESTING:
Other: ________________________________
Fetal Ultrasound Abnormality
(please specify below and attach copy of fetal ultrasound)
Parental Sample:
Brain malformation: ___________________________________
Maternal Blood: 5-10mL EDTA
Facial cleft: _________________________________________
Heart defect: ________________________________________
Paternal Blood: 5-10mL EDTA
Lung abnormality:_____________________________________
Diaphragmatic hernia: _________________________________
GI abnormality:_______________________________________
SPECIMEN COLLECTION:
GU abnormality:______________________________________
Skeletal abnormality: __________________________________
NT greater than or equal to 3.5mm: _______________________
Date: _____________________________
(DD/MM/YYYY)
Other: ______________________________________________
Time: _____________________________
Known familial microarray deletion/duplication syndrome
(provide copy of the result)
CVH Lab Use Only
Date Rec’d:(DD/MM/YYYY) _______________________ Time: _________________ # Tubes Rec’d: _________________
Comments: __________________________________________________________________________________________
Unit #
LAB #
PRENATAL MICROARRAY REQUISITION

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