Pages that link to "Q38540463"
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The following pages link to Carpenter's syndrome: Acrocephalopolysyndactyly. An autosomal recessive syndrome (Q38540463):
Displaying 34 items.
- Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization (Q24300813) (← links)
- RAB23 mutations in Carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesity (Q24305935) (← links)
- Webbed fingers (Q24531983) (← links)
- Acrocephalopolysyndactyly type IV: A new genetic syndrome in 3 sibs* (Q28237928) (← links)
- A new syndrome with acrocephalopolysyndactyly, cardiac disease, and distinctive defects of the ear, skin, and lower limbs (Q28238304) (← links)
- Normal intelligence in two children with carpenter syndrome (Q28267030) (← links)
- Bardet-Biedl and Laurence-Moon syndromes in a mixed Arab population (Q28296930) (← links)
- Ophthalmic Features of Cransosynostosis (Q30445458) (← links)
- A sporadic case of apparent Crouzon's syndrome with extracraniofacial manifestations. (Q33586099) (← links)
- Prevention of heart disease in infants and children (Q35434054) (← links)
- Genetic, hypothalamic and endocrine features of clinical and experimental obesity (Q35655934) (← links)
- Association of Congenital Heart Disease with Syndromes or Other Defects (Q35879938) (← links)
- A Novel Aberrant Splice Site Mutation in RAB23 Leads to an Eight Nucleotide Deletion in the mRNA and Is Responsible for Carpenter Syndrome in a Consanguineous Emirati Family (Q36600658) (← links)
- A review of hedgehog signaling in cranial bone development (Q36732493) (← links)
- The Laurence-Moon-Biedl syndrome. Six cases of obesity, short stature, mental retardation, small genitalia, and retinitis pigmentosa (Q38538373) (← links)
- Carpenter's syndrome. Report of a case (Q38539317) (← links)
- Classification and evaluation of the obesities. (Q38597669) (← links)
- Apert's syndrome--a report of five cases (Q39360445) (← links)
- Craniosynostosis. Review of the literature and indications for surgery (Q39889820) (← links)
- Genetic Disorders Associated with Mental Retardation: Clinical Aspects (Q39931176) (← links)
- Apert's syndrome (acrocephalosyndactyly). A description and a report on seven cases (Q39956794) (← links)
- The Greig polysyndactyly-craniofacial dysmorphism syndrome (Q40117325) (← links)
- Genetics of obesity in humans and animal models (Q41284438) (← links)
- Hearing loss in Pfeiffer's syndrome (Q50598904) (← links)
- Hydrocephalus and mental retardation in craniosynostosis (Q52081305) (← links)
- A new craniodigital syndrome with mental retardation (Q52122786) (← links)
- Classification of craniosynostosis (Q56334485) (← links)
- A case of Carpenter syndrome diagnosed in a 20‐week‐old fetus with postmortem examination (Q56381028) (← links)
- Carpenter syndrome with normal intelligence and precocious growth (Q56417977) (← links)
- (Q56420370) (← links)
- Clinocephaly:Considerations on the pathophysiology of Craniosynostosis (Q56421086) (← links)
- Frontodigital syndrome: a dominantly inherited disorder with normal intelligence (Q57931080) (← links)
- Syndromology: an updated conceptual overview. X. References (Q67291615) (← links)
- Heptacarpo-octatarso-dactyly combined with multiple malformations (Q70760117) (← links)