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Links

The following are links to some external web sites that may be able to provide you with information about various chromosomal and genetic diseases.

Support Groups/Parent Organizations

Angelman Syndrome Foundation
Association for Retarded Citizens

Canavan Research Foundation

Chicago Center for Jewish Genetic Disorders

Chromosome 18 Registry & Research Society

Cystic Fibrosis Foundation

Down Syndrome Family Empowerment Network

Dysautonomia Foundation

Fabry Support and Information Group

Factor V Leiden Activated Protein C and Activated Protein S Support Page

Familial Dysautonomia Hope Foundation

Five P- Society (Cri du Chat Syndrome)

Genetic Alliance

March of Dimes

National Down Syndrome Society

National Fragile X Foundation

National Gaucher Foundation

National Hemophilia Foundation

National MPS Society

National Niemann-Pick Disease Foundation

National Organization for Rare Disorders

National Tay Sachs and Allied Diseases

National Parent to Parent Network

Our Kids

Prader-Willi Alliance of New York

SOFT (Support for Trisomy 13/18)

Spina Bifida Association of America

Turner's Syndrome

UCSF-Stanford Lysosomal Disease Center

Upside! Down Syndrome Society

Williams Syndrome Association


Related Information

We have developed a number of educational materials to help patients better understand their testing options.

AFP3 - Afp4 (PDF)
Amniocentesis (PDF)

Carrier Screening for Persons of Ashkenazi Jewish Descent (PDF)

Chorionic Villi Sampling (PDF)

Cystic Fibrosis (PDF)

Directions for Mouthwash Sample Collection (PDF)

Fragile X (PDF)

FirstScreen (PDF)

IntegratedScreen (PDF)

Patient Billing (PDF)

Preimplantation Genetic Diagnosis (PGD) (PDF)

Serum
IntegratedScreen (PDF)

Spinal Muscular Atrophy (SMA) (PDF)

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