YHRD – Y Chromosome Haplotype Reference Database
Y-STR Haplotype Reference Database
U.S. Department of Energy Genome Program
Single Nucleotide Polymorphisms Database
Short Tandem Repeat Internet Database
PubMed: Biomedical Literature Citations and Abstracts
Orphanet
On-line Mendelian Inheritance in Man (OMIM)
OBGYN.net
National Centre for Biotechnological Information
GENDIA
GeneTests
Forensic Chromosome X Research
ENFSI DNA WG STR Population Database
EDNAP Mitochondrial DNA Population Database
E.C.A. Register of Unbalanced Chromosome Aberrations (ECARUCA)
Cytogenetic Resources
Cytogenetics (Pathology Server)
Ciência Hoje, ciência e tecnologia em directo
Chromosome help station (for families with rare chromosome disorders)
Frequency of Inherited Disorders Database
European Directory of DNA laboratories
Chromosomal Variation in Man Online
The Cancer Genome Anatomy Project (CGAP)
Cancer Chromosomes (Cytogenetic Databases)
Atlas of Genetics and Cytogenetics in Oncology and Haematology
Sociedade Portuguesa de Células Estaminais e Terapia Celular
Sociedade Portuguesa de Bioquímica
Sociedade Portuguesa de Medicina da Reprodução
Sociedade Portuguesa de Obstetrícia e Ginecologia
Organização Mundial de Saúde (OMS)
Ordem dos Médicos
Ordem dos Biólogos
The Fetal Medicine Foundation
International Society for Forensic Genetics (ISFG)
Grupo Espanhol e Português da Sociedade Internacional de Genética Forense (GEP-ISFG)
European Society of Human Reproduction and Embryology
European Society of Human Genetics
European DNA Profiling Group (EDNAP)
EuroGentest
DNA Learning Center
Direcção Geral de Saúde (DGS)
Cystic Fibrosis Foundation
British Society for Human Genetics
Association of Genetic Technologists
Association des Cytogénéticiens de Langue Française (ACFL)
Associação Portuguesa de Diagnóstico Pré-Natal
Associação Nacional de Bioquímicos
American Society of Human Genetics
American Society of Gene Therapy
American College of Medical Genetics (ACMG)
Alliance of Genetic Support Groups
Access Excellence @ The National Health Museum
