Detalhe da pesquisa
1.
Heterozygous deletion of the VEGFC gene in 4q34.3 is associated with Milroy-like lymphedema: First prenatal case report.
Am J Med Genet A
; 188(12): 3550-3554, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36129367
2.
Should prenatal chromosomal microarray analysis be offered for isolated fetal growth restriction? A French multicenter study.
Am J Obstet Gynecol
; 225(6): 676.e1-676.e15, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34058167
3.
Exome sequencing identifies the first genetic determinants of sirenomelia in humans.
Hum Mutat
; 41(5): 926-933, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32058622
4.
Screening for small for gestational age infants in early vs late third-trimester ultrasonography: a randomized trial.
Am J Obstet Gynecol MFM
; 5(11): 101162, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37717697
5.
Hyperechoic metaphyses in hypophosphatasia: what does it mean?
Pediatr Radiol
; 38(3): 340-3, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18084754