Publication | Closed Access
Identification of de novo deletions at the NF1 gene: no preferential paternal origin and phenotypic analysis of patients
49
Citations
29
References
1997
Year
Phenotypic AnalysisMendelian DisorderGenetic DisorderGeneticsNf1 GenePathologyMolecular GeneticsPreferential Paternal OriginGenomicsDisease Gene IdentificationMedicine
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