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Library / Personalized Information Packets

Download original chromosome chapters and brochures below or request a personalized information packet. Each rare chromosome or gene mutation disorder is highly specific. That is why CDO offers personalized information packets to our members based upon the details contained in their genetic analyses reports. General information may be helpful but it can also provide conflicting specifics that might be confusing or even alarming in some instances. The information contained in each CDO packet has been either selected and approved by our consulting geneticist. And we always urge follow-up with personal healthcare providers should there be further questions or concerns.

To request an information packet please contact us.  Packets available only to current CDO Members. To Join or Renew your membership please click here

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Brochures (English)

1p31.3 Deletion Syndrome

1p36 Deletion Syndrome

1q21.1 Deletion Syndrome

1q43-q44 Deletion Syndrome

2q33 Deletion

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3q21 Deletions

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3q26.33 Deletions

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3q29 Deletion Syndrome

5p13.2 Deletion (Cornelia de Lange Syndrome)

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5q14.3 Deletion

5q35 Duplication

6q25.1 Deletion

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6q26-6q27 Deletions

7q21.3 Deletion

8p11 Deletions

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10q24 Duplication

10q26 deletion

14q12 Deletion
(FOXG1-Syndrome)

14q23 Deletions

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15q11.2 Deletion (Burnside-Butler Syndrome)

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15q24.2 Deletion (Witteveen-Kolk Syndrome)

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15q26 Deletion

16p11.2
microdeletion

16p11.2 microduplication

17p13.3 Duplication

22q11.2 Deletion Syndrome

Alagille Syndrome
and Deletion 20p12

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Alfi Syndrome

BPES Syndrome

Cat Eye Syndrome

CHARGE Syndrome

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Cri du Chat
Syndrome

Distal 18q Deletion

Emanuel Syndrome

Feingold Syndrome 1
Deletion 2p24

HDR (Barakat) Syndrome

Jacobsen Syndrome

KBG Syndrome &
16q24.3 Deletion

Kleefstra
Syndrome

Koolen-de Vries Syndrome

Lamb-Shaffer Syndrome

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Langer Giedion Syndrome

Klinefelter Syndrome

Malan Syndrome

Pitt-Hopkins Syndrome

Ring Chromosome 14

San Luis Valley Syndrome

Smith-Magenis Syndrome

Trisomy 9p

Tetrasomy 18p

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Townes-Brocks Syndrome

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Uniparental Disomy

Waardenburg Syndrome

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WAGR Syndrome

Williams Syndrome

Wolf-Hirschhorn

Xq28 Duplication Syndrome

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Folletos (Español)

Sindrome de Delecion1p36
Monosomía 1p36

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