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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Noonan syndrome associated with growth hormone deficiency with biallelic LZTR1 variants

Full text
Author(s):
Nakaguma, Marilena [1] ; Jorge, Alexander A. L. [2] ; Arnhold, Ivo J. P. [1]
Total Authors: 3
Affiliation:
[1] Univ Sao Paulo, Unidade Endocrinol Desenvolvimento, Lab Hormonios & Genet Mol LIM42, Hosp Clin, Disciplina Endocrinol, Fac Med, Sao Paulo - Brazil
[2] Univ Sao Paulo, Unidade Endocrinol Genet, Lab Endocrinol Celular & Mol LIM25, Hosp Clin, Disciplina Endocrinol, Fac Med, Sao Paulo - Brazil
Total Affiliations: 2
Document type: Letter
Source: Genetics in Medicine; v. 21, n. 1, p. 260, JAN 2019.
Web of Science Citations: 3
Abstract

FAPESP's process: 13/03236-5 - New approaches and methodologies in molecular-genetic studies of growth and pubertal development disorders
Grantee:Alexander Augusto de Lima Jorge
Support Opportunities: Research Projects - Thematic Grants
FAPESP's process: 13/02162-8 - Molecular pathogenesis and characterization of monogenic developmental diseases: a route to translational medicine
Grantee:Berenice Bilharinho de Mendonça
Support Opportunities: Research Projects - Thematic Grants
FAPESP's process: 15/26563-7 - Molecular genetic diagnosis in patients with pituitary and gonadal developmental disorders and the use of models in vitro and in vivo to evaluate the functional effect of allelic variants identified by sequencing large scale
Grantee:Luciani Renata Silveira de Carvalho
Support Opportunities: Regular Research Grants