Pages that link to "Q40226242"

The following pages link to The Tay syndrome (congenital ichthyosis with trichothiodystrophy). (Q40226242):

Displaying 17 items.

• Syndromic (phenotypic) diarrhea in early infancy (Q21202896) (← links)
• Trichothiodystrophy: a systematic review of 112 published cases characterises a wide spectrum of clinical manifestations (Q24633351) (← links)
• Neurology and the skin (Q24673115) (← links)
• Dysregulation of the peroxisome proliferator-activated receptor target genes by XPD mutations (Q33884120) (← links)
• Trichothiodystrophy: Photosensitive, TTD-P, TTD, Tay Syndrome (Q34129840) (← links)
• International classification of osteochondrodysplasias. The International Working Group on Constitutional Diseases of Bone (Q36312563) (← links)
• Magnetic resonance imaging pattern recognition in hypomyelinating disorders (Q36661277) (← links)
• Tay or IBIDS Syndrome: A Case with Growth and Mental Retardation, Congenital Ichthyosis and Brittle Hair (Q36939703) (← links)
• Tay syndrome (Q51960807) (← links)
• Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity (Q52077519) (← links)
• Prenatal diagnosis of PIBIDS (Q67785367) (← links)
• Trichothiodystrophy, xeroderma pigmentosum and PIBI(D)S syndrome (Q68257785) (← links)
• Trichothiodystrophy without photosensitivity. Biochemical, ultrastructural and DNA repair studies (Q68449431) (← links)
• PIBI(D)S syndrome--trichothiodystrophy with xeroderma pigmentosum (group D) mutation (Q69026646) (← links)
• PIBIDS: Tay's syndrome and xeroderma pigmentosum (Q70061208) (← links)
• [Collodion baby with neonatal signs of trichothiodystrophy misdiagnosed as Netherton syndrome: reassessment of a previous diagnostic error] (Q80051072) (← links)
• PIBI(D)S syndrome: a new entity with defect of the deoxyribonucleic acid excision repair system (Q93660945) (← links)