E-LIB Suche - Ergebnisse für: Britt, Allison

1

O27: Utility of cfDNA in comprehensive genomic profiling of..:

Li, Dong ; Sheppard, Sarah ; March, Michael...
Genetics in Medicine Open. 2 (2024) - p. 101020 , 2024

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

2

P783: Two fetuses with hereditary hemorrhagic telangiectasi..:

Burrill, Natalie ; Teefey, Christina Paidas ; Kumar, Nankee...
Genetics in Medicine Open. 2 (2024) - p. 101691 , 2024

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

3

Complex lymphatic anomalies: Molecular landscape and medica..:

Borst, Alexandra J. ; Britt, Allison ; Adams, Denise M.
Seminars in Pediatric Surgery. 33 (2024) 3 - p. 151422 , 2024

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

4

Expanding Genetic Counselor Roles: A Model for Global Resea..:

Muraresku, Colleen C. ; McCormick, Elizabeth M. ; Rockart, Lydia...
Genes. 15 (2024) 7 - p. 867 , 2024

Link: https://doi.org/10.3390/..

5

Mosaic pathogenic variants in AKT3 cause capillary malforma..:

Bolli, Amber ; Nriagu, Bede ; Britt, Allison D....
American Journal of Medical Genetics Part A. 191 (2023) 5 - p. 1442-1446 , 2023

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

6

Microcystic lymphatic malformations in Turner syndrome are ..:

Nriagu, Bede N. ; Williams, Lydia S. ; Brewer, Niambi...
American Journal of Medical Genetics Part A. 194 (2023) 1 - p. 64-69 , 2023

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

7

Genomic profiling informs diagnoses and treatment in vascul..:

Li, Dong ; Sheppard, Sarah E. ; March, Michael E....
Nature Medicine. 29 (2023) 6 - p. 1530-1539 , 2023

Link: https://doi.org/10.1038/..

8

262. Acute Posttraumatic Somatic and Psychological Symptoms..:

Britt, Allison ; Li, Qinghua ; An, Xinming...
Biological Psychiatry. 93 (2023) 9 - p. S199 , 2023

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

9

Double aneuploidy mosaicism involving chromosomes 18 and 21..:

Mendiola, Christina ; Ortega, Veronica ; Britt, Allison..
Molecular Cytogenetics. 15 (2022) 1 - p. , 2022

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

10

GH1 C.291 + 34G>C in a Growth Hormone Deficient Pedigree:

Vidal, Katherine ; Britt, Allison D ; George, Anu..
Journal of the Endocrine Society. 5 (2021) Supplement_1 - p. A558-A558 , 2021

Link: https://doi.org/10.1210/..

11

Copy neutral absence of heterozygosity on chromosome 15 dis..:

Ortega, Veronica ; Louie, Raymond J. ; Jones, Melanie A....
Molecular Cytogenetics. 14 (2021) 1 - p. , 2021

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

12

Phenotypes Associated with 16p11.2 Copy Number Gains and Lo..:

Chu, Caleb ; Wu, Haotian ; Xu, Fangling...
Laboratory Medicine. 51 (2020) 6 - p. 642-648 , 2020

Link: https://doi.org/10.1093/..

13

A De novo HDAC2 variant in a patient with features consiste..:

Wagner, Victoria F. ; Hillman, Paul R. ; Britt, Allison D...
American Journal of Medical Genetics Part A. 179 (2019) 5 - p. 852-856 , 2019

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

14

Genotypic and phenotypic variability of 22q11.2 microduplic..:

Yu, Alexander ; Turbiville, Donald ; Xu, Fangling...
American Journal of Medical Genetics Part A. 179 (2019) 11 - p. 2178-2189 , 2019

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

15

Cover Image, Volume 176A, Number 4, April 2018:

Zarate, Yuri A. ; Smith‐Hicks, Constance L. ; Greene, Carol...
American Journal of Medical Genetics Part A. 176 (2018) 4 - p. , 2018

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