Pages that link to "Q35118706"
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The following pages link to Idiopathic infantile hypercalcaemia--a continuing enigma (Q35118706):
Displaying 50 items.
- Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growth (Q24675777) (← links)
- Radio-ulnar synostosis in Williams syndrome. A frequently associated anomaly (Q28241527) (← links)
- The calcitonin-CGRP gene in the infantile hypercalcaemia/Williams-Beuren syndrome (Q33593298) (← links)
- Unbalanced 13;18 translocation and Williams syndrome (Q33593677) (← links)
- Williams-Beuren syndrome: an update and review for the primary physician (Q33634325) (← links)
- Williams syndrome (Q33673673) (← links)
- Williams-Beuren syndrome: phenotypic variability and deletions of chromosomes 7, 11, and 22 in a series of 52 patients (Q33678087) (← links)
- Prevalence of scoliosis in Williams-Beuren syndrome patients treated at a regional reference center (Q33846320) (← links)
- Williams (Williams Beuren) syndrome: a distinct neurobehavioral disorder (Q33942663) (← links)
- Hyperacusis, sound annoyance, and loudness hypersensitivity in children (Q34007777) (← links)
- Familial Williams-Beuren syndrome showing varying clinical expression (Q34136369) (← links)
- Natural history of Williams syndrome: physical characteristics (Q34406298) (← links)
- Personality characteristics and behaviour problems in individuals of different ages with Williams syndrome (Q34439067) (← links)
- Hypercalcemia in infants presenting with apnea. (Q34578508) (← links)
- Clinical and molecular cytogenetic (FISH) diagnosis of Williams syndrome (Q34798831) (← links)
- Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markers. (Q35087211) (← links)
- Williams syndrome: an update on clinical and molecular aspects (Q35264833) (← links)
- Vitamin D metabolites in idiopathic infantile hypercalcaemia (Q35602605) (← links)
- Age at diagnosis and abilities in idiopathic hypercalcaemia (Q35603475) (← links)
- Cardiac anomalies in Williams-Beuren syndrome (Q35604951) (← links)
- A clinical study of Noonan syndrome (Q35627319) (← links)
- New height, weight and head circumference charts for British children with Williams syndrome (Q36155499) (← links)
- How much vitamin D for children? (Q36333484) (← links)
- Genome wide array-CGH and qPCR analysis for the identification of genome defects in Williams' syndrome patients in Saudi Arabia (Q37169363) (← links)
- Cytochrome P450-mediated metabolism of vitamin D. (Q37590269) (← links)
- Description of common musculoskeletal findings in Williams Syndrome and implications for therapies (Q38691495) (← links)
- Hypercalcemia in Patients with Williams-Beuren Syndrome. (Q38803879) (← links)
- A Pediatric Patient with a CYP24A1 Mutation: Four Years of Clinical, Biochemical, and Imaging Follow-Up (Q39230407) (← links)
- Endocrine control and disturbances of calcium and phosphate metabolism in children (Q39669611) (← links)
- Psychopathological and behavior impairments in Williams-Beuren syndrome: the influence of gender, chronological age, and cognition. (Q40012360) (← links)
- A cognitive and behavioural phenotype in williams syndrome (Q43422369) (← links)
- Progressive vascular lesions in Williams-Beuren syndrome (Q43606406) (← links)
- Beyond behaviour: is social anxiety low in Williams syndrome? (Q50307277) (← links)
- Environmental sound recognition by timbre in children with Williams syndrome. (Q50695681) (← links)
- What can we learn from old microdeletion syndromes using array-CGH screening? (Q50795886) (← links)
- Treatment of children with Williams syndrome with methylphenidate (Q51102902) (← links)
- Renal and urinary findings in 20 patients with Williams-Beuren syndrome diagnosed by fluorescence in situ hybridization (FISH). (Q51935674) (← links)
- Independence and adaptive behavior in adults with Williams syndrome. (Q52001340) (← links)
- Neurologic findings in children and adults with Williams syndrome (Q52011151) (← links)
- Procedural learning deficit in children with Williams syndrome. (Q52020188) (← links)
- Myopathy in Williams-Beuren syndrome. (Q52050527) (← links)
- Fluorescent in situ hybridization (FISH) as a diagnostic tool for Williams-Beuren syndrome (Q57978091) (← links)
- Chiari I malformation in asymptomatic young children with Williams syndrome: clinical and MRI study (Q59629747) (← links)
- Statural growth in Williams-Beuren syndrome (Q67575503) (← links)
- Increased serum level of 1,25-dihydroxyvitamin D3 after parathyroid hormone in the normocalcemic phase of idiopathic hypercalcemia (Q68371960) (← links)
- The middle aortic syndrome: an important feature of Williams' syndrome (Q73298241) (← links)
- Williams-Beuren syndrome 35 years after the diagnosis in one of the first Beuren patients (Q73680947) (← links)
- [Maternal stress among mothers of children with Williams-Beuren syndrome, Down's syndrome and mental retardation of non-syndromal etiology in comparison to mothers of non-disabled children] (Q77409036) (← links)
- Elevated ambulatory blood pressure in 20 subjects with Williams syndrome (Q77416146) (← links)
- Longitudinal evaluation of growth, puberty, and bone maturation in children with Williams syndrome (Q77765239) (← links)