CMYK 0.000000 CMYK 0.000000 ZTPnXwAH3AI5tI12J0EvmicCUokavBZqWdfiotI1qXCtyH3UybWtPl3zB6pkHm2+ELUKp6GneG/x Reproductive carrier screening provides information about your chance of having a child with a serious genetic condition. 50.000000 0.000000 qH4moBv0rNrTmw1S6hs44L6+83yXKEPIIIpUdh6ZVwxuJXpQjcKepHHffAlE2lz6bGNNR85cJA7u It may lead to a range of physical and emotional reactions, especially if there are decisions that need to be made. 0 In the past, the only clue that a healthy person was a carrier had been the diagnosis of a genetic condition in their child. 30.000000 90.000000 0.000000 0.000000 AiE3dFHc9NuvhjaqX/KvfJ3B3Pk/Wh8KqYRPCK8AqAjjd8SSrnv05fS2tPV0ACKACoAAodyPn1yK C=50 M=100 Y=0 K=0 Fulgent Genetics may not be bound by laws that provide the same level of protection for personal information afforded by the Australian Privacy Principles (APPs). AQACAwQFBgcICQoLEAACAQMDAgQCBgcDBAIGAnMBAgMRBAAFIRIxQVEGE2EicYEUMpGhBxWxQiPB 68jx6e06BAbWbU6EgFalUmTt9kfsDYeOHw8cfo+6mMss5/USfjacp5V8zhZIjrchiBPoEHVOacgR CMYK Oxygen >Couples tested by Sonic Genetics and found to be at high risk of having an affected child will be offered genetic counselling free-of-charge,^ upon referral from your doctor. 95.000000 Please use our dedicated request form for the Beacon expanded carrier screen. CMYK CMYK Cyan 1 0 obj <>/OCGs[16 0 R]>>/Pages 3 0 R/Type/Catalog>> endobj 2 0 obj <>stream Version 2.050;PS 2.000;hotconv 1.0.51;makeotf.lib2.0.18671 PROCESS The Beacon Expanded + Opt-In carrier screening is the largest pan-ethnic screening panel available. 35.000000 0.000000 4.998800 20.000000 50.000000 10.000000 saved gSp/p7y4ocTWHlZGofSrbXvJVBLFiHRCSCyqVBBqH8KBVQudf0V4JJ1sPKz/AB+oa298zCOR1Eck 0.000000 The Beacon expanded reproductive carrier screen tests more than 400 genes to identify if you are a carrier of a genetic condition that could affect your baby. CMYK CMYK 17KdQKCo7UIHgaDDYQ9GFaCpqe5GwrkUuxV2KuxV2KuxV2KuxV2KuIDAgioOxB6UxV4b5p8y38Hm PROCESS False CMYK 792.000000 100.000000 Adobe Illustrator CC 2017 (Macintosh) +DlJWWl5iZmpucnZ6fkqOkpaanqKmqq6ytrq+v/aAAwDAQACEQMRAD8A9U4q7FXYq7FVOG5tpwxg lCOPavzq/BVWPR72K5jlT8zIX+qK0U8Ml5I42LOSx+s/b4q1ajalabbD4K1ZaHqSXtT+ZkNxJEOM 0.000000 Roboto-Light 0.000000 CMYK This delay could be due to three reasons: We apologise for any delay in reporting your genetic test result. iVB3Oxxq0g0Xmfljztqt5dRWk1/pN0xQmV47e4nkbgeHKKOKKAFXJB5VIB+GgOMYEcyT8kymDyAH Open Type The chromosomes are made of DNA, the chemical that encodes the genes in every cell of your body. CMYK 50.000000 PROCESS JFKkryBFRXuMVeeD8j/LsscZi1O6CemI2mjMRZ+LcuVSrLyqSeQXlXeviRO1MaUV/wCcf/LKkOmo Regular OypyJPxbud/fphsoR6/k/wCVEYGK2liC1osd5OgAJ5EDiBxB8BQfcKDiTSbL5A8q8I1k0Oym9MUD nJ0hVfzLJFIFh87aluSkUissoVHdm/erNeENwUU5CjdvixpU702a6uNFe4bVfNd4pi+C5sW5LwWR Payment is required before the test is performed. Medium qbnJ2en5KjpKWmp6ipqqusra6voRAAICAQIDBQUEBQYECAMDbQEAAhEDBCESMUEFURNhIgZxgZEy jUvy/k0CfS/r+lQ6TdKwkSK+jjB9UsSQy0PJmVvpBx3VJdN8kfllqFyYdJure4uApd4bPU2kbjsr CMYK application/pdf saved OmyNJEZ52deJF1cTXC9a1Cys6g+4GHdjYZBbNUN9GACmUSrYWTsVdirsVdir/9k= PROCESS C=100 M=90 Y=0 K=0 FbsSehxV45aaF55S2Kyafq6yys7yySXsTmOq1X06QleJpSlBx7A5OwgKY8v+dIZZJIdP1/0VDPHE 14 Giffnock Avenue, Macquarie Park NSW 2113. and that both partners have their own fully completed request form signed by each other. PROCESS PROCESS 75.000000 CMYK > Individual testing - Females are tested for more than 400 genes; this includes more than 50 genes on the X chromosome. gtQDRPOhtpQ0MYLOwKEEKFZGJp2DA+G+KvEdM8peSppWmv8ATda9Zf8AeUWkU6Qeg8YUKyzyzguR C=40 M=70 Y=100 K=50 +WxO0ToJwJ1Zm5AryozbUUAip+dMbCrn8sefIzHFb6F5daCMgAAXEf7sAUUAO1CKUrv16Cm7YV6b 10.000000 50.000000 C=0 M=50 Y=100 K=0 CMYK There is no Medicare rebate for carrier screening. HKQwuzVL0Uk+3bJCWX+aPmwMY96qPOdk7cEt9QLgVKDTb8kd6U9DDxZP5o+bHhHf9iq/meFH4vDf The Beacon expanded reproductive carrier screen tests more than 400 genes to identify if you are a carrier of a genetic condition that could affect your baby. 39.999400 Oxygen 0.000000 CMYK 0.000000 Sonic Genetics assessed the value of each test by calculating the proportion of Australian couples who would be identified as being at high risk of having a child with an autosomal recessive or X-linked recessive disorder (see Figure).

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