Publication | Closed Access
Contiguous gene syndrome due to an interstitial deletion in Xp22.3 in a boy with ichthyosis, chondrodysplasia punctata, mental retardation and ADHD
41
Citations
13
References
2007
Year
Developmental BiologyGenetic DisorderGeneticsContiguous Gene SyndromePathologyMolecular GeneticsDisease Gene IdentificationInterstitial DeletionAbnormal DevelopmentMental RetardationMedicineMonogenic Disorders
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