E-LIB Suche - Ergebnisse für: Jordan, Valerie K.

1

Running a successful STEMM summer program: A week‐by‐week g..:

Beasley, Heather K. ; Vue, Zer ; McReynolds, Melanie R....
Journal of Cellular Physiology. , 2024

2

SOX7 deficiency causes ventricular septal defects through i..:

Hernández-García, Andrés ; Pendleton, Katherine E ; Kim, Sangbae...
Human Molecular Genetics. 32 (2023) 13 - p. 2152-2161 , 2023

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

3

RERE deficiency contributes to the development of orofacial..:

Kim, Bum Jun ; Zaveri, Hitisha P ; Kundert, Peter N...
Human Molecular Genetics. 30 (2021) 7 - p. 595-602 , 2021

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

4

RERE deficiency leads to decreased expression of GATA4 and ..:

Kim, Bum Jun ; Zaveri, Hitisha P. ; Jordan, Valerie K....
Disease Models & Mechanisms. 11 (2018) 9 - p. , 2018

Link: https://doi.org/10.1242/..

5

Genotype-phenotype correlations in individuals with pathoge..:

Jordan, Valerie K. ; Fregeau, Brieana ; Ge, Xiaoyan...
Human Mutation. 39 (2018) 5 - p. 666-675 , 2018

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

6

The role of FREM2 and FRAS1 in the development of congenita..:

Jordan, Valerie K ; Beck, Tyler F ; Hernandez-Garcia, Andres...
Human Molecular Genetics. 27 (2018) 12 - p. 2064-2075 , 2018

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

7

Duplication of HEY2 in cardiac and neurologic development:

Jordan, Valerie K. ; Rosenfeld, Jill A. ; Lalani, Seema R..
American Journal of Medical Genetics Part A. 167 (2015) 9 - p. 2145-2149 , 2015

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

8

FBN1 contributing to familial congenital diaphragmatic hern..:

Beck, Tyler F. ; Campeau, Philippe M. ; Jhangiani, Shalini N....
American Journal of Medical Genetics Part A. 167 (2015) 4 - p. 831-836 , 2015

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

9

Genotype–phenotype correlations in individuals with pathoge..:

Jordan, Valerie K ; Fregeau, Brieana ; Ge, Xiaoyan...
qt57z6f57h. , 2018

Link: https://escholarship.org..

10

Genotype–phenotype correlations in individuals with pathoge..:

Jordan, Valerie K ; Fregeau, Brieana ; Ge, Xiaoyan...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903952/. , 2018

Link: http://www.ncbi.nlm.nih...

11

De Novo Mutations of RERE Cause a Genetic Syndrome with Fea..:

Fregeau, Brieana ; Kim, Bum Jun ; Hernández-García, Andrés...
qt0rd5k1p2. , 2016

Link: https://escholarship.org..

12

De Novo Mutations of RERE Cause a Genetic Syndrome with Fea..:

Fregeau, Brieana ; Kim, Bum Jun ; Hernández-García, Andrés...
0002-9297. , 2016

Link: https://dspace.library.u..

13

Duplication of HEY2 in Cardiac and Neurologic Development:

Jordan, Valerie K ; Rosenfeld, Jill A ; Lalani, Seema R.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4545384/. , 2015

Link: http://www.ncbi.nlm.nih...

14

FBN1 Contributing to Familial Congenital Diaphragmatic Hern..:

Beck, Tyler F ; Campeau, Philippe M ; Jhangiani, Shalini N...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4522925/. , 2015

Link: http://www.ncbi.nlm.nih...

15

1p36 deletion syndrome: an update:

Jordan, Valerie K ; Zaveri, Hitsha P ; Scott, Daryl A
info:eu-repo/semantics/altIdentifier/doi/10.2147/TACG.S65698. , 2015

Link: https://www.dovepress.co..