Detalhe da pesquisa
1.
COVID contingencies: Early epicenter experiences of different genetics clinics at a New York City institution inform emergency adaptation strategies.
J Genet Couns
; 30(4): 938-948, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33734519
2.
Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal Rearrangements.
Am J Hum Genet
; 101(2): 206-217, 2017 Aug 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28735859
3.
Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
Lancet
; 393(10173): 758-767, 2019 02 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-30712878
4.
Telehealth for High-Risk Pregnancies in the Setting of the COVID-19 Pandemic.
Am J Perinatol
; 37(8): 800-808, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32396948
5.
Telehealth Uptake into Prenatal Care and Provider Attitudes during the COVID-19 Pandemic in New York City: A Quantitative and Qualitative Analysis.
Am J Perinatol
; 37(10): 1005-1014, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32516816
6.
Structural Chromosomal Rearrangements Require Nucleotide-Level Resolution: Lessons from Next-Generation Sequencing in Prenatal Diagnosis.
Am J Hum Genet
; 99(5): 1015-1033, 2016 Nov 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27745839
7.
Parental perceptions of prenatal whole exome sequencing (PPPWES) study.
Prenat Diagn
; 38(11): 801-811, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30035818
8.
3' UTR Deletion of FBXO28 in a Patient with Brain Abnormalities and Developmental Delay.
Genes (Basel)
; 14(9)2023 08 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37761828
9.
Tay-Sachs Carrier Screening by Enzyme and Molecular Analyses in the New York City Minority Population.
Genet Test Mol Biomarkers
; 20(9): 504-9, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27362553
10.
Rare inheritance of Leri-Weill Syndrome due to crossover of short stature Homeobox Gene (SHOX) Deletions between X and Y Chromosomes: a case report.
Int J Pediatr Endocrinol
; 2013(1): 11, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23809065