Detalhe da pesquisa
1.
Fetal Hemoglobin H Hydrops Fetalis: Another Three Case Reports.
Hemoglobin
; 47(2): 102-104, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37247248
2.
Can placental extracellular vesicles provide long-term protection against cardiovascular disease?
Am J Obstet Gynecol
; 230(6): e125, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38408621
3.
δ-Thalassemia with Complete Absence of Hb A2 in a Chinese Family.
Hemoglobin
; 42(2): 135-137, 2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29737888
4.
Newborn screening for Hb H disease by determination of Hb Bart's using the Sebia capillary electrophoresis system in southern China.
Hemoglobin
; 38(1): 73-5, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24229410
5.
Chromosomal microarray analysis detects trisomy 9 mosaicism in a prenatal case not revealed by conventional cytogenetic analysis of cord blood.
J Obstet Gynaecol
; 39(1): 123-125, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-29560757
6.
Codon 62 (GTG>GCG, ValâAla) (α1) (HBA1: c.188T>C) causing nondeletional α-thalassemia in a Chinese family.
Hemoglobin
; 37(2): 188-91, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23470151
7.
Hb J-Wenchang-Wuming [α11(A9)LysâGln (AAG>CAG) (α2 or α1)] compromises neonatal screening for α-thalassemia with the Sebia Capillarys2 electrophoresis system.
Hemoglobin
; 36(4): 395-8, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22680346
8.
A novel case of Hb Phnom Penh: codons 117/118 (+ATC) as a cause of α+ -thalassemia.
Hemoglobin
; 36(3): 289-92, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22432594
9.
Screening for common nondeletional α-thalassemias in Chinese newborns by determination of Hb Bart's using the Sebia Capillarys 2 electrophoresis system.
Hemoglobin
; 36(2): 196-9, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22239481
10.
A novel α-thalassemia frameshift mutation: codon 8 (-C).
Hemoglobin
; 36(2): 192-5, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22242813
11.
Chromosomal microarray analysis in pregnancies at risk for a molecular disorder.
J Matern Fetal Neonatal Med
; 34(1): 159-162, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-30651013
12.
Can cell-free DNA testing be used in pregnancies with isolated fetal omphalocele? Preliminary evidence from cytogenetic results of prenatal cases.
J Matern Fetal Neonatal Med
; 34(4): 624-628, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31018788
13.
Fetoscopic repair of spina bifida: continued refinement of the procedure is needed.
Am J Obstet Gynecol MFM
; 5(4): 100894, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36758678
14.
Apparent germline mosaicism for a 15q11-q13 deletion causing recurrent Angelman syndrome in a Chinese family.
Eur J Obstet Gynecol Reprod Biol
; 236: 255-257, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30890277
15.
Newborn screening for α-thalassaemia by a capillary electrophoresis method.
J Med Screen
; 19(3): 159; author reply 159-60, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23093733