Results 1 -
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1,246
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genetic testing
- ... dominant inheritance pattern. Atrial fibrillation, familial Auricular fibrillation Genetic Testing Registry: Atrial fibrillation, familial, 1 Genetic Testing Registry: ...
- ... the condition. Dysencephalia splanchnocystica Meckel-Gruber syndrome MKS Genetic Testing Registry: Meckel syndrome, type 1 Genetic Testing Registry: Meckel syndrome, type 6 Genetic Testing Registry: ...
- ... X chromosome Turner-like syndrome Ullrich-Noonan syndrome Genetic Testing Registry: Noonan syndrome Genetic Testing Registry: Noonan syndrome 1 Genetic Testing Registry: Noonan ...
- ... signs and symptoms of the condition. NPH NPHP Genetic Testing Registry: Nephronophthisis 1 Genetic Testing Registry: Infantile nephronophthisis Genetic Testing Registry: Nephronophthisis Genetic ...
- ... symptoms of the condition. DeSanctis-Cacchione syndrome XP Genetic Testing Registry: ERCC1-Related Xeroderma Pigmentosum Genetic Testing Registry: Xeroderma pigmentosum group B Genetic Testing Registry: ...
- ... Rod body disease Rod myopathy Rod-body myopathy Genetic Testing Registry: Actin accumulation myopathy Genetic Testing Registry: Congenital myopathy 23 Genetic Testing Registry: Congenital ...
- ... Right ventricular dysplasia, arrhythmogenic Ventricular dysplasia, right, arrhythmogenic Genetic Testing Registry: Arrhythmogenic right ventricular cardiomyopathy Genetic Testing Registry: ...
- ... symptoms of the condition. Immotile cilia syndrome PCD Genetic Testing Registry: Primary ciliary dyskinesia Genetic Testing Registry: Primary ciliary dyskinesia 10 Genetic Testing Registry: ...
- ... abiotrophy Leber congenital tapetoretinal degeneration Leber's amaurosis Genetic Testing Registry: Leber congenital amaurosis Genetic Testing Registry: Leber ...
- ... is usually unknown. Parkinson disease PD Primary parkinsonism Genetic Testing Registry: Autosomal dominant Parkinson disease 1 Genetic Testing Registry: Autosomal dominant Parkinson disease 4 Genetic Testing ...