Meet Linden (12536)

Linden is attractive with an athletic, lean, muscular build; lightly tan skin; sandy brown hair; and hazel eyes. He has youthful yet masculine features with a rectangular face, rosy cheeks, dark pink lips, square chin, and medium-sized nose.

Linden is a focused and determined student who hopes to start a career in business finance after graduation. He is a quiet yet charismatic, likable, down-to-earth guy who enjoys running, working out, watching football, and frequent visits to Hawaii to enjoy the nice weather and outdoors.



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IUI Units

43 Vials Available

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Audio Interview
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Baby Photos
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Extended Profile
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Keirsey Test
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Staff Impression
Genetic Test Results
All Access Pass Membership

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All Donor Materials Included

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Meet Linden (12536)

Linden is attractive with an athletic, lean, muscular build; lightly tan skin; sandy brown hair; and hazel eyes. He has youthful yet masculine features with a rectangular face, rosy cheeks, dark pink lips, square chin, and medium-sized nose.

Linden is a focused and determined student who hopes to start a career in business finance after graduation. He is a quiet yet charismatic, likable, down-to-earth guy who enjoys running, working out, watching football, and frequent visits to Hawaii to enjoy the nice weather and outdoors.

Brown/Green

Light Brown

178

73

B Rh+

-

Caucasian, German, Irish

No

B.A. Business Administration / Student

Yes

Counsyl Foresight Panel (at least 175 conditions)


A lab called Igenomix offers custom carrier screening to patients in the UK, called Carrier Genetic Test, Synchronized (CGT SYNC). Igenomix will custom design the carrier screening panel to confirm your compatibility with a specific donor. Please simply click on this link and select “CTG” as the service in the dropdown menu to request information. A genetic counselor from Igenomix will reach out to you with additional information. Or you can email the Igenomix genetic counselors at [email protected] if you would like to proceed with the CGT Sync testing or have any questions. This is not a mandated requirement, and is fully at the discretion of the patient to utilize this service, or not.


    • Cerebrotendinous Xanthomatosis : Carrier
    • Spinal Muscular Atrophy : No disease causing mutations detectedative result: No disease causing mutations detectedative for g.27134T>G SNP and SMN1: 2 copies.
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