E-LIB Suche - Ergebnisse für: Schwartz, Stuart

1

P592: Cytogenetic and microarray analysis of prenatally det..:

Schwartz, Stuart ; Arreola, Alexandra ; Gadi, Inder...
Genetics in Medicine Open. 2 (2024) - p. 101498 , 2024

Link: https://doi.org/10.1016/..

2

P140: A rare phenomenon: Double trisomy rescue detected dur..:

Penton, Andrea ; Papenhausen, Peter ; Schwartz, Stuart..
Genetics in Medicine Open. 2 (2024) - p. 101037 , 2024

Link: https://doi.org/10.1016/..

3

Prenatal detection of mosaicism for a genome wide uniparent..:

Johansen, Margriet ; Haskell, Gloria T. ; Arreola, Alexandra...
Prenatal Diagnosis. 44 (2024) 5 - p. 586-594 , 2024

Link: https://doi.org/10.1002/..

4

P571: Detection of isodisomy utilizing SNP microarray: Freq..:

Molinari, Sharon ; Williams, Niecy ; Phillips, Karen...
Genetics in Medicine Open. 2 (2024) - p. 101477 , 2024

Link: https://doi.org/10.1016/..

5

P479: Mosaicism for genome wide homozygosity identified as ..:

Haskell, Gloria ; Askree, Hussain ; Kline, Laura...
Genetics in Medicine Open. 1 (2023) 1 - p. 100526 , 2023

Link: https://doi.org/10.1016/..

6

Uniparental disomy of multiple chromosomes in two cases wit..:

Polonis, Katarzyna ; Lopes, Jaime L. ; Cabral, Huong...
American Journal of Medical Genetics Part A. 191 (2023) 7 - p. 1978-1983 , 2023

Link: https://doi.org/10.1002/..

7

Laboratory performance of genome-wide cfDNA for copy number..:

Soster, Erica ; Tynan, John ; Gibbons, Clare...
Molecular Cytogenetics. 16 (2023) 1 - p. , 2023

Link: https://doi.org/10.1186/..

8

O36: Moving on from cytogenetics: The evolution from squash..:

Schwartz, Stuart ; Arreola, Alexandra ; Gadi, Inder...
Genetics in Medicine Open. 1 (2023) 1 - p. 100462 , 2023

Link: https://doi.org/10.1016/..

9

10. SNP microarray analysis of over 7,500 myeloid patients:..:

Schwartz, Stuart ; Thomason, Ronald ; Dong, Henry.
Cancer Genetics. 260-261 (2022) - p. 4 , 2022

Link: https://doi.org/10.1016/..

10

Navigating choice in the face of uncertainty: using a theor..:

Castillo, Gisell ; Lalu, Manoj M ; Asad, Sarah...
BMJ Open. 11 (2021) 3 - p. e043929 , 2021

Link: https://doi.org/10.1136/..

11

Clinical significance and mechanisms associated with segmen..:

Papenhausen, Peter R. ; Kelly, Carla A. ; Harris, Samuel...
Molecular Cytogenetics. 14 (2021) 1 - p. , 2021

Link: https://doi.org/10.1186/..

12

Hematologists' barriers and enablers to screening and recru..:

on behalf of the GO CART team ; Castillo, Gisell ; Lalu, Manoj...
Trials. 22 (2021) 1 - p. , 2021

Link: https://doi.org/10.1186/..

13

4. ETV6-ABL1 variant rearrangement described in a childhood..:

Arreola, Alexandra ; Papenhausen, Peter R. ; Gadi, Inder K...
Cancer Genetics. 252-253 (2021) - p. S2 , 2021

Link: https://doi.org/10.1016/..

14

Partnering with patients to get better outcomes with chimer..:

Foster, Madison ; Fergusson, Dean A ; Hawrysh, Terry...
Research Involvement and Engagement. 6 (2020) 1 - p. , 2020

Link: https://doi.org/10.1186/..

15

Deletion rescue resulting in segmental homozygosity: A mech..:

Caldwell, Samantha ; Sagaser, Katelynn ; Nelson, Zoe...
American Journal of Medical Genetics Part A. 182 (2020) 11 - p. 2666-2670 , 2020

Link: https://doi.org/10.1002/..