Pages that link to "Q39088657"
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The following pages link to X-linked ichthyosis, bilateral cryptorchidism, hypogenitalism and mental retardation in two siblings (Q39088657):
Displaying 4 items.
- An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometry (Q24678018) (← links)
- Clinical spectrum of steroid sulfatase deficiency: X-linked recessive ichthyosis, birth complications and cryptorchidism (Q40090712) (← links)
- Genetic heterogeneity of the ichthyosis, hypogonadism, mental retardation, and epilepsy syndrome. Clinical and biochemical investigations on two patients with Rud syndrome and review of the literature (Q40228728) (← links)
- Syndromes of ichthyosis and related disorders (Q67463309) (← links)