Variability in clinical phenotype despite common chromosomal deletion in Smith-Magenis syndrome [del(17)(p11.2p11.2)] - Concepedia

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Variability in clinical phenotype despite common chromosomal deletion in Smith-Magenis syndrome [del(17)(p11.2p11.2)]

113

Citations

26

References

2003

Year

Lorraine Potocki, Christine J. Shaw, Paweł Stankiewicz, James R. Lupski

Genetics in Medicine

Genetic DisorderGeneticsHematologyGenetic EpidemiologyPathologyMolecular GeneticsMedical GeneticsClinical PhenotypeDisease Gene IdentificationMedicineCommon Chromosomal DeletionClinical Genetics

References

	Year	Citations

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