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familial diseases
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OMIM - Congenital disorder
OMIM - Metabolic disease
OMIM - Multisystem Complex Disorders
OMIM - Cancer
Mouse Phenotypes - Autosomal dominant hereditary disorder
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AutozygosityMapper: Identification of disease-mutations in consanguineous families.
Measures for optimal access to psychosocial care of children with rare diseases and their families].
Genetic services survey-experience of people with rare diseases and their families accessing genetic…
Advance care planning to patients with chronic kidney disease and their families: An intervention de…
Internet research of utilization of social media in patients with urological disease and their famil…
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Psychosocial Situation of Children With Rare (Congenital) Pediatric Surgical Diseases and Their Fami…
Efficacy of a Multicomponent and Interdisciplinary Intervention on the Care Ability and Burden of Fa…
Clinical and Molecular Studies in Families With Glaucoma and Related Diseases
Genetic and Family Studies of Inherited Muscle Diseases
Clinical and Genetic Studies in Families With Myopia and Related Diseases
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