Detalhe da pesquisa
1.
Severe Craniofacial Involvement due to Amniotic Band Sequence.
Fetal Pediatr Pathol
; 37(1): 27-37, 2018 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-29336649
2.
Effects of SPTA1 Gene Variants on the Hematological Phenotype of Mexican Patients with Hereditary Spherocytosis.
Genet Test Mol Biomarkers
; 26(5): 270-276, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35638908
3.
Microcephaly, an etiopathogenic vision.
Pediatr Neonatol
; 62(4): 354-360, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34112604
4.
Clinical Exome Sequencing Enables Congenital Sialidosis Type II Diagnosis in Two Siblings Presenting with Unreported Clinical Features from a Rare Homozygous Sequence Variant p.(Tyr370Cys) in NEU1.
Mol Syndromol
; 12(4): 250-257, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-34421504
5.
Whole-exome sequencing in three children with sporadic Blau syndrome, one of them co-presenting with recurrent polyserositis.
Autoimmunity
; 53(6): 344-352, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32597225
6.
A 9p13-->p24 duplication coupled with a whole 22q translocation onto 9p24.
J Appl Genet
; 48(1): 95-8, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17272869
7.
Causas del hidrops fetal: experiencia en un hospital obstétrico del Occidente de México / Etiology of fetal hydrops: experience in an obstetric hospital in western Mexico
Ginecol. obstet. Méx
; 90(7): 579-589, ene. 2022. tab, graf
Artigo
em Espanhol
|
LILACS-Express
| ID: biblio-1404946