Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations (2004)
- Authors:
- USP affiliated authors: MENDONÇA, BERENICE BILHARINHO DE - FM ; LEITE, CLAUDIA DA COSTA - FM
- Unidade: FM
- Subjects: MUTAÇÃO GENÉTICA; GLÂNDULA PITUITÁRIA (ANORMALIDADES;DEFICIÊNCIA); SEQUENCIAMENTO GENÉTICO; HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA)
- Language: Inglês
- Imprenta:
- Publisher: International Society of Endocrinology
- Publisher place: Lisboa
- Date published: 2004
- Source:
- Título do periódico: Program and Abstracts
- Conference titles: International Congress of Endocrinology
-
ABNT
MELO, M. E. et al. Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 16 abr. 2024. -
APA
Melo, M. E., Marui, S., Leite, C. C., Mendonca, B. B., & knoepfelmacher, M. (2004). Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations. In Program and Abstracts. Lisboa: International Society of Endocrinology. -
NLM
Melo ME, Marui S, Leite CC, Mendonca BB, knoepfelmacher M. Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations. Program and Abstracts. 2004 ;[citado 2024 abr. 16 ] -
Vancouver
Melo ME, Marui S, Leite CC, Mendonca BB, knoepfelmacher M. Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations. Program and Abstracts. 2004 ;[citado 2024 abr. 16 ] - Ressonancia magnética e função hipofisaria em pacientes com deficiência de GH com E sem mutações nos genes GH-1, receptor do GHRH-R e HESX-1
- Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe
- Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes
- Novel heterozygous nonsesns GLI2 mutations in patientswith hypopituitarism and ectopic posterios pituitary lobe without holoprosencephaly
- Frequent development of combined pituitary hormone deficiency in patients initially diagnosed as isolated growth hormone deficiency: a long term follow-up of patients from a single center
- The benign spectrum of hypothalamic hamartomas: Infrequent epilepsy and normal cognition in patients presenting with central precocious puberty
- Espasmo de acomodação persistente após trauma craniano grave de lente de contato do Hewa: achados à imagem por ressonância magnética em dois pacientes
- Pharyngeal dimensions in healthy men and women
- Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
- Absense of duplication on DAX1 gene in patients with 46,XY sex reversal
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