Phenotypic Features and Response to GH Treatment of Patients With a Molecular Defect of the IGF-1 Receptor | Zendy

M.J.E. Walenkamp | Zendy; Jasmijn M L Robers | Zendy; Jan M. Wit | Zendy; Gladys R.J. Zandwijken | Zendy; Hermine A. van Duyvenvoorde | Zendy; Wilma Oostdijk | Zendy; Anita Hokken-Koelega | Zendy; Sarina G. Kant | Zendy; Monique Losekoot | Zendy

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Phenotypic Features and Response to GH Treatment of Patients With a Molecular Defect of the IGF-1 Receptor

Author(s) -

M.J.E. Walenkamp,

Jasmijn M L Robers,

Jan M. Wit,

Gladys R.J. Zandwijken,

Hermine A. van Duyvenvoorde,

Wilma Oostdijk,

Anita Hokken-Koelega,

Sarina G. Kant,

Monique Losekoot

Publication year - 2019

Publication title -

the journal of clinical endocrinology and metabolism

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 2.206

H-Index - 353

eISSN - 1945-7197

pISSN - 0021-972X

DOI - 10.1210/jc.2018-02065

Subject(s) - short stature , insulin like growth factor 1 receptor , medicine , endocrinology , microcephaly , small for gestational age , phenotype , pediatrics , birth weight , gastroenterology , pregnancy , biology , receptor , genetics , growth factor , gene

The phenotype and response to GH treatment of children with an IGF1R defect is insufficiently known.

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