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1.
Clinical and molecular characterization of 10 Chinese children with congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency.
World J Pediatr
; 2023 Jul 24.
Artículo
en Inglés
| MEDLINE | ID: mdl-37486441
2.
Circulating circular RNA profiles associated with celiac disease seropositivity in children with type 1 diabetes.
Front Pediatr
; 10: 960825, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36210930
3.
Alström syndrome with a novel mutation of ALMS1 and Graves' hyperthyroidism: A case report and review of the literature.
World J Clin Cases
; 9(13): 3200-3211, 2021 May 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-33969109
4.
Correction to: Clinical and molecular characterization of 10 Chinese children with congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency.
World J Pediatr
; 2024 Jan 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-38240902
5.
[Association of 45, X/46, XY mosaicism with disorders of sex development: the clinical analysis of 5 cases].
Zhonghua Er Ke Za Zhi
; 49(6): 451-4, 2011 Jun.
Artículo
en Zh
| MEDLINE | ID: mdl-21924060
6.
[Long-term follow-up of isolated-growth hormone deficiency typeIA: the clinical analysis of 2-sister cases].
Zhonghua Er Ke Za Zhi
; 48(12): 944-6, 2010 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-21215191
7.
[Genetic mutation analysis of a kindred with a patient suffering from 17 alpha-hydroxylase/17, 20-lyase deficiency].
Zhonghua Er Ke Za Zhi
; 47(10): 789-91, 2009 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-20021817
8.
[Identification of a novel missense mutation of the DAX-1 gene in a Chinese pedigree with X-linked adrenal hypoplasia congenita].
Zhonghua Er Ke Za Zhi
; 45(12): 937-41, 2007 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-18339285
9.
[Prader-Willi syndrome and genomic imprinting].
Zhonghua Er Ke Za Zhi
; 41(6): 453-6, 2003 Jun.
Artículo
en Zh
| MEDLINE | ID: mdl-14749005
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