![Genetic genealogy / Medical genetics / Mental retardation / RPS6KA3 / X-linked mental retardation / Rare diseases / Ribosomal s6 kinase / Sensorineural hearing loss / Fryns Syndrome / Health / Syndromes / Coffin–Lowry syndrome Genetic genealogy / Medical genetics / Mental retardation / RPS6KA3 / X-linked mental retardation / Rare diseases / Ribosomal s6 kinase / Sensorineural hearing loss / Fryns Syndrome / Health / Syndromes / Coffin–Lowry syndrome](https://www.pdfsearch.io/img/4b44c7e2912c0fa37db0e78d21e61fb8.jpg)
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City Hoboken / Young / / Company Hunter AG / Siris E. & Wegenkia L.C. / Temtamy S.A. / / MedicalCondition loss of consciousness / cranial hyperostosis / microcephaly / drop attacks / non syndromic X-linked mental retardation / RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome / sensorineural hearing loss / mitral valve dysfunction / pneumonia / mental retardation / injury / Obesity / spinal kyphosis/scoliosis / Lowry syndrome / schizophrenia / disease / Epilepsy / Coffin-Lowry syndrome / hypotonia / dominant gene mental retardation syndrome / psychiatric illness / only non-syndromic mental retardation / myocarditis / convulsion / depression / X-linked mental retardation / inherited faciodigital mental retardation syndrome / orbital hypertelorism / epileptic seizures / / Organization FOR THE STUDY OF BEHAVIOURAL PHENOTYPES An International Organisation The SSBP / Registered Charity / / Person André Hanauer / / Product clonazepam / /
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