Publication | Closed Access
Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delay
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References
1998
Year
Developmental AnomalyDevelopmental BiologyMendelian DisorderGenetic DisorderMedicineGeneticsNeurofibromatosis Type 1Maternal OriginNeuroscienceDisease Gene IdentificationAbnormal DevelopmentNeuropathologyMonogenic DisordersNeurogeneticsGross Deletions
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