Detalhe da pesquisa
1.
[Molecular diagnostic tests for thrombophilia in patients referred to genetic counseling clinic because due to recurrent pregnancy failure. One center's experience]. / Badania molekularne w kierunku trombofilii u pacjentek skierowanych do poradni genetycznej z powodu niepowodzen ciazowych. Doswiadczena jednego osrodka.
Ginekol Pol
; 83(3): 178-82, 2012 Mar.
Artigo
Polonês
| MEDLINE | ID: mdl-22568192
2.
Clinical Importance of aCGH in Genetic Counselling of Children with Psychomotor Retardation.
Appl Clin Genet
; 15: 27-38, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35603035
3.
Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 Pregnancies.
Genes (Basel)
; 13(4)2022 04 14.
Artigo
Inglês
| MEDLINE | ID: mdl-35456496
4.
Wide Fontanels, Delayed Speech Development and Hoarse Voice as Useful Signs in the Diagnosis of KBG Syndrome: A Clinical Description of 23 Cases with Pathogenic Variants Involving the ANKRD11 Gene or Submicroscopic Chromosomal Rearrangements of 16q24.3.
Genes (Basel)
; 12(8)2021 08 17.
Artigo
Inglês
| MEDLINE | ID: mdl-34440431
5.
Prenatal identification of partial 3q duplication syndrome.
BMC Med Genomics
; 12(1): 85, 2019 06 13.
Artigo
Inglês
| MEDLINE | ID: mdl-31196198