Detalhe da pesquisa
1.
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder.
Am J Hum Genet
; 111(5): 996, 2024 May 02.
Artigo
Inglês
| MEDLINE | ID: mdl-38701747
2.
DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable Immunodeficiency.
Am J Hum Genet
; 103(6): 1038-1044, 2018 12 06.
Artigo
Inglês
| MEDLINE | ID: mdl-30503519
3.
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder.
Am J Hum Genet
; 103(2): 221-231, 2018 08 02.
Artigo
Inglês
| MEDLINE | ID: mdl-30057030
4.
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder.
Am J Hum Genet
; 103(3): 456, 2018 09 06.
Artigo
Inglês
| MEDLINE | ID: mdl-30193137
5.
Resolving the heterogeneity of diaphragmatic mesenchyme: a novel mouse model of congenital diaphragmatic hernia.
Dis Model Mech
; 14(1)2021 01 26.
Artigo
Inglês
| MEDLINE | ID: mdl-33735101
6.
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume.
Nat Commun
; 10(1): 357, 2019 01 21.
Artigo
Inglês
| MEDLINE | ID: mdl-30664637
7.
Fifty shades of white: Understanding heterogeneity in white adipose stem cells.
Adipocyte
; 6(3): 205-216, 2017 07 03.
Artigo
Inglês
| MEDLINE | ID: mdl-28949833
8.
Isolation and Fluorescence-Activated Cell Sorting of Murine WT1-Expressing Adipocyte Precursor Cells.
Methods Mol Biol
; 1467: 81-91, 2016.
Artigo
Inglês
| MEDLINE | ID: mdl-27417961