McCune-Albright syndrome: a longitudinal clinical study of 32 patients. - Wikidata - wikimedia - TriplyDB

McCune-Albright syndrome: a longitudinal clinical study of 32 patients.

McCune-Albright syndrome: a longitudinal clinical study of 32 patients.

http://www.wikidata.org/entity/Q33805772

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MEN1, MEN4, and Carney Complex: Pathology and Molecular Genetics Somatic GNAS mutation causes widespread and diffuse pituitary disease in acromegalic patients with McCune-Albright syndrome Constitutive expression of Gsα(R201C) in mice produces a heritable, direct replica of human fibrous dysplasia bone pathology and demonstrates its natural history.Characterization and management of testicular pathology in McCune-Albright syndrome.A Case of Atypical McCune-Albright Syndrome with Vaginal Bleeding Genomic imprinting and dermatological disease.McCune-Albright syndrome and disorders due to activating mutations of GNAS1.A newly recognized polyosteolysis/hyperostosis syndrome.A case of big bad bones.Sudden infant death syndrome and activating GNAS1 gene mutations

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P2860

McCune-Albright syndrome: a longitudinal clinical study of 32 patients.

http://www.wikidata.org/entity/Q33805772

description

1999 nî lūn-bûn

@nan

1999 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

1999 թվականի նոյեմբերին հրատարակված գիտական հոդված

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1999年の論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年论文

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name

McCune-Albright syndrome: a longitudinal clinical study of 32 patients.

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McCune-Albright syndrome: a longitudinal clinical study of 32 patients.

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McCune-Albright syndrome: a longitudinal clinical study of 32 patients.

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McCune-Albright syndrome: a longitudinal clinical study of 32 patients.

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McCune-Albright syndrome: a longitudinal clinical study of 32 patients.

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McCune-Albright syndrome: a longitudinal clinical study of 32 patients.

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JPEM.1999.12.6.817

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Journal of Pediatric Endocrinology and Metabolism

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McCune-Albright syndrome: a longitudinal clinical study of 32 patients.

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P2093

Balsamo A

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Bergamaschi R

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Bertelloni S

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Buzi F

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Cappa M

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Cisternino M

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Franzese A

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Ghizzoni L

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Lala R

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Lucci M

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P2860

Standards from birth to maturity for height, weight, height velocity, and weight velocity: British children, 1965. II.

Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndrome.

Severe endocrine and nonendocrine manifestations of the McCune-Albright syndrome associated with activating mutations of stimulatory G protein GS.

A case of neonatal McCune-Albright syndrome with Cushing syndrome and hyperthyroidism.

Nonparametric Estimation from Incomplete Observations

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10614538

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