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Analysis per medical speciality
ARRAY CGC Molecular Diagnosis of Noonan Syndrome and other Genetically Related Syndromes
Array CGC for Craniosynostosis
ARRAY CGC Molecular Diagnosis of Bardet-Biedl Syndrome
ARRAY CGC for Skeletal Dysplasia
PND plus +
ARRAY CGC Molecular Diagnosis of Congenital Hearing Loss (combined)
Array CGC Thrombophilia
ARRAY CGC Molecular Diagnosis of Metabolic Disorders
ARRAY CGC Molecular Diagnosis of Nonsyndromic Congenital Hearing Loss
ARRAY CGC Molecular Diagnosis of Syndromic Congenital Hearing Loss
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Last update, 2010/08/06
