Large asymptomatic adrenal haematomas in the neonate

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Asn540Lys mutation in fibroblast growth factor receptor 3 and phenotype in hypochondroplasia.

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Mutations in short stature homeobox containing gene (SHOX) in dyschondrosteosis but not in hypochondroplasia.

Human genetics·2000

A microdeletion in 19q13.2 associated with mental retardation, skeletal malformations, and Diamond-Blackfan anaemia suggests a novel contiguous gene syndrome.

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A novel missense mutation Ile538Val in the fibroblast growth factor receptor 3 in hypochondroplasia. Mutations in brief no. 122. Online.

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Long-term prognosis of post-infectious renal scarring in relation to radiological findings in childhood--a 27-year follow-up.

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Cardiovascular responses to the intracarotid injections of ionic contrast media and iohexol in the dog.

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Computed chest tomography in rats with pulmonary damage due to microembolism.

Acta radiologica: diagnosis·1986

Value of bone scan in the McCune-Albright syndrome. Report of a case.

Acta radiologica: diagnosis·1986

Inadvertently performed hysterosalpingography during early pregnancy.

Acta radiologica: diagnosis·1986

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Acta radiologica: diagnosis·1986

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Journal of perinatology : official journal of the California Perinatal Association·2026

Variants of varying clinical consequence (VVCCs) are associated with differing penetrance and expressivity in children with CRMS/CFSPID.

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society·2026

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Tracheopexy for Severe Tracheobronchomalacia in Children with Bronchopulmonary Dysplasia: A Two-Center Study of Patient Characteristics and Outcomes.

Journal of pediatric surgery·2026

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Large asymptomatic adrenal haematomas in the neonate

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Analysis of short stature homeobox-containing gene ( SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity.

Asn540Lys mutation in fibroblast growth factor receptor 3 and phenotype in hypochondroplasia.

Mutations in short stature homeobox containing gene (SHOX) in dyschondrosteosis but not in hypochondroplasia.

A microdeletion in 19q13.2 associated with mental retardation, skeletal malformations, and Diamond-Blackfan anaemia suggests a novel contiguous gene syndrome.

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