Detalhe da pesquisa
1.
Non-invasive prenatal testing for trisomy 21 based on analysis of cell-free fetal DNA circulating in the maternal plasma.
Prenat Diagn
; 35(5): 471-6, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25643828
2.
Building operational readiness for responding to emergencies in the WHO South-East Asia Region.
WHO South East Asia J Public Health
; 9(1): 37-42, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32341220
3.
Approaches to the diagnosis and grading of hiatal hernia.
Best Pract Res Clin Gastroenterol
; 22(4): 601-16, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18656819
4.
Deletion of CPEB1 Gene: A Rare but Recurrent Cause of Premature Ovarian Insufficiency.
J Clin Endocrinol Metab
; 101(5): 2099-104, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27003306
5.
An innovative self-care module for palliative care medical learners.
J Palliat Med
; 16(6): 603-8, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23631613
6.
[Anonymous sperm donation does not increase the risk for unions between relatives nor the incidence of autosomal recessive diseases due to consanguinity]. / Le don anonyme de sperme n'augmente pas significativement les unions entre apparentés, la consanguinité et l'incidence des maladies récessives.
Gynecol Obstet Fertil
; 42(4): 200-4, 2014 Apr.
Artigo
em Francês
| MEDLINE | ID: mdl-24679600
7.
Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations.
Neurology
; 73(12): 962-9, 2009 Sep 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-19770472