Shopping Resources - Genetic Disorders

Companies that offer products and services related to Genetic Disorders should be in our directory which currently contains more than 2 million listings. We do our best to deliver results at waar-is.com so you get the most relevant information available today in the NL for your search for Genetic Disorders.

Top>Health>Conditions and Diseases>Genetic Disorders>

> Aarskog Syndrome
> Aase Syndrome
> Ablepharon-Macrostomia Syndrome
> Alagille Syndrome
> Alkaptonuria
> Alpha-1 Antitrypsin Deficiency
> Batten
> Beckwith-Wiedemann Syndrome
> Coffin Lowry Syndrome
> Costello Syndrome
> Cowden Syndrome
> Craniofrontonasal Dysplasia
> Crigler-Najjar Syndrome
> Cystic Fibrosis
> DiGeorge Syndrome
> Down Syndrome
> Dubowitz Syndrome
> Ectodermal Dysplasia
> Familial Hypercholesterolemia
> Fatty Oxidation
> Floating-Harbor Syndrome
> Fragile X Syndrome
> Glutaricaciduria
> Hailey-Hailey Disease
> Hemihypertrophy
> Hemochromatosis
> Hereditary Angioedema
> Hereditary Spastic Paraplegia
> Incontinentia Pigmenti
> Joubert Syndrome
> Klinefelter Syndrome
> Laurence-Moon Syndrome
> Lesch-Nyhan Syndrome
> Lowe Syndrome
> Machado-Joseph
> Mannosidosis
> McArdle's
> Meckel-Gruber Syndrome
> Mobius Syndrome
> Nail Patella Syndrome
> Noonan Syndrome
> Opitz Syndrome
> Organizations
> Pallister Killian Mosaic Syndrome
> Pallister-Hall Syndrome
> Personal Pages
> Popliteal Pterygium Syndrome
> Prader-Willi Syndrome
> Propionic Acidemia
> Proteus Syndrome
> Prune Belly Syndrome
> Pseudoxanthoma Elasticum
> Robinow Syndrome
> Russell Silver Syndrome
> Sanfilippo Syndrome
> Schizencephaly
> Shwachman Syndrome
> Smith Lemli Opitz Syndrome
> Smith-Magenis Syndrome
> Soto's Syndrome
> Sturge-Weber Syndrome
> Thrombocytopenia Absent Radius Syndrome
> Turner Syndrome
> Urea Cycle
> Usher Syndrome
> Velo-Cardio-Facial Syndrome
> Von Hippel-Lindau
> Waardenburg Syndrome
> Weaver Syndrome
> Williams Syndrome
> Xeroderma Pigmentosum
> Zellweger Syndrome

1. Chromosome Help-Station: For people with rare chromosome diso...

Welcome to the Chromosome Help-Station! for people with rare chromosome disorders The purpose of this site is tosupport and advise people with rare chromosome disorders, their families and organisations. EUROCHROMNET MEET EUROPEAN NETWORKS FOR RARE C...
http://www.chromosomehelpstation.com/

2. Ohne Titel

http://home.planet.nl/~lette111/

3. WEB-PAGINA van NICO J. LESCHOT

FUNCTIES: Hoogleraar Klinische Genetica aan de Universiteit van Amsterdam (UVA) Hoofd van de afdeling Klinische Genetica in het Academisch Medisch Centrum Plv. opleider voor het medisch specialisme Klinische Genetica (MSRC) Medecoördinator basiscursus v...
http://home.tiscali.nl/~leschot/

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Blepharophimosis Ptosis Epicanthus Inversus Syndrome

The BPEI (BPES) Family Network encourages people to get in touch with each other, share information and ask questions. Explanation of this rare eye disorder.
(http://freespace.virgin.net/andy.bowles/)

Dr. Greene's HouseCalls

A discussion of medical information on trisomy, trisomy 13, genetics, and his own personal family experience with this rare disease.
(http://www.drgreene.com/html/21614.html)

Gene Clinics

Medical genetics knowledge base. NIH funded, expert-authored descriptions of inherited disorders. Covers genetic testing in diagnosis and management and genetic counseling of patients.
(http://www.geneclinics.org)

Genetic and Rare Conditions Site

Lay advocacy groups, support groups, information on genetic conditions and birth defects for professionals, educators and individuals. Disorders from A-Z.
(http://www.kumc.edu/gec/support/)

Genetic Disorders: The Links to Diet

Explores the role of diet in birth defects and genetic disorders. Includes nutritional links to disorders such as Down syndrome, cerebral palsy, homocystinuria, and cystic fibrosis.
(http://www.ctds.info/genetic_disorders.html)

IMMD Institute of Medical Molecular Diagnostics Ltd.

The IMMD is a genetic testing laboratory located in Germany. Provides genetic tests for hereditary breast cancer, various cardiovascular diseases or diseases with onset in childhood.
(http://www.immd.de/)

Primary Ciliary Dyskinesia

Information on a rare congenital disease.
(http://www.p-c-d.org/en/)

The UDGD Spot

Resources and information for families of children with genetic disabilities or syndromes that are still awaiting a diagnosis.
(http://www.camp-a-roo.com/UDGD/)

Washington University in St Louis

Family resource for individuals with Papillon Lefevre, Haim-Munk Syndrome and Prepubertal Periodontis. Interested families may participate in a registry dedicated to learning about the natural history of these three conditions.
(http://www.siteman.wustl.edu/physician/clinical_trials/non_t)

XLH Network

Patient support group for XLH, a genetic condition also known as X-Linked Hypophosphatemia, X-Linked Hypophosphatemic Rickets, Familial Hypophosphatemia, Vitamin D-Resistant Rickets.
(http://www.xlhnetwork.org)

Your Genes, Your Health

The DNA Learning Center's multimedia guide to genetic disorders. Complete in depth articles about each disease listed.
(http://www.ygyh.org)

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