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door Taria
28 mei 2020, 07:19
Forum: Open forum
Onderwerp: Snijder-Blok Campaeu Syndrom CHD3 Mutation
Reacties: 2
Weergaves: 7085

Snijder-Blok Campaeu Syndrom CHD3 Mutation

Hello from Germany! My son Jaron (9 years old) has in addition to a distinctive Pierre Robin Sequence, a lot of other disbilities with unknown reason. After years of searching, a human geneticist diagnosed the „Snijder-Blok Campaeu Syndrom“ / CHD3 mutation. I´m looking for contact for an exchange wi...