E-LIB Suche - Ergebnisse für: Crotwell, Patricia L.

1

Mutation in GM2A Leads to a ProgressiveChorea-dementia Synd..:

Salih, Mustafa A. ; Seidahmed, Mohammed Z. ; El Khashab, Heba Y....
Tremor and Other Hyperkinetic Movements. 5 (2015) 0 - p. 306 , 2015

Link: https://doi.org/10.5334/..

2

Congenital nasal pyriform aperture stenosis and ocular albi..:

Somsen, David ; Davis‐Keppen, Laura ; Crotwell, Patricia...
American Journal of Medical Genetics Part A. 164 (2014) 5 - p. 1268-1271 , 2014

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

3

Mutations in VLDLR associated with ataxia with secondary vi..:

Kruer, Michael C. ; Jepperson, Tyler N. ; Weimer, Jill M....
Movement Disorders. 28 (2013) 13 - p. 1904-1905 , 2013

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

4

Advances in Whole-Genome Genetic Testing: From Chromosomes ..:

Crotwell, Patricia L. ; Hoyme, H. Eugene
Current Problems in Pediatric and Adolescent Health Care. 42 (2012) 3 - p. 47-73 , 2012

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

5

Prenatally diagnosed trisomy 20 mosaicism associated with a..:

Stein, Quinn P. ; Boyle, Jeffrey G. ; Crotwell, Patricia L....
Prenatal Diagnosis. 28 (2008) 12 - p. 1169-1170 , 2008

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

6

Gene expression patterns underlying proximal–distal skeleta..:

Crotwell, Patricia L. ; Mabee, Paula M.
Developmental Dynamics. 236 (2007) 11 - p. 3111-3128 , 2007

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

7

Expression of bmp2a and bmp2b in late-stage zebrafish media..:

Crotwell, Patricia L. ; Sommervold, Amber R. ; Mabee, Paula M.
Gene Expression Patterns. 5 (2004) 2 - p. 291-296 , 2004

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

8

Evolution of median fin modules in the axial skeleton of fi..:

Mabee, Paula M. ; Crotwell, Patricia L. ; Bird, Nathan C..
Journal of Experimental Zoology. 294 (2002) 2 - p. 77-90 , 2002

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

9

Gdf5 is expressed in the developing skeleton of median fins..:

Crotwell, Patricia ; Clark, Tim ; Mabee, Paula
Development Genes and Evolution. 211 (2001) 11 - p. 555-558 , 2001

Link: https://doi.org/10.1007/..

10

THE WONDERFUL WORLD OF CICHLIDS:

CROTWELL, PATRICIA
BioScience. 51 (2001) 5 - p. 410 , 2001

Link: https://doi.org/10.1641/..

11

The first patient with tandem duplication of 6q14q16: Molec..:

Sanmann, Jennifer N. ; Casas, Kari A. ; Bevilacqua, Jen...
American Journal of Medical Genetics Part A. 170 (2016) 9 - p. 2416-2420 , 2016

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

12

HOMOZYGOUS GNAL MUTATION ASSOCIATED WITH FAMILIAL CHILDHOOD..:

MYERS, Angela ; Padilla-Lopez, Sergio ; Dursun, ALİ...
45057f47-6b7a-4611-99c0-12f936cd685b. , 2016

Link: https://doi.org/10.1212/..

13

Homozygous Gnal Mutation Associated With Familial Childhood..:

Masuho, Ikuo ; Fang, Mingyan ; Geng, Chunyu...
10.1212/NXG.0000000000000078. , 2016

Link: http://hdl.handle.net/11..

14

Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-D..:

Madeo, Marianna ; Stewart, Michelle ; Sun, Yuyang...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4908178/. , 2016

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

15

Homozygous GNAL mutation associated with familial childhood..:

Masuho, Ikuo ; Fang, Mingyan ; Geng, Chunyu...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4866576/. , 2016

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