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Yang, Sandra
3034
results:
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Online (3034)
Mediatypes
E-Books (2)
Articles (Online) (913)
Bookchapter (Online) (48)
OpenAccess-fulltext (2071)
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english (2632)
german (1)
more...
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1
Clinical utility of exome sequencing in infantile heart fai..:
Ritter, Alyssa
;
Bedoukian, Emma
;
Berger, Justin H.
...
Genetics in Medicine. 22 (2020) 2 - p. 423-426 , 2020
Link:
https://doi.org/10.1038/..
?
2
Phenotypic spectrum and transcriptomic profile associated w..:
Castilla-Vallmanya, Laura
;
Selmer, Kaja K.
;
Dimartino, Clémantine
...
Genetics in Medicine. 22 (2020) 7 - p. 1215-1226 , 2020
Link:
https://doi.org/10.1038/..
?
3
Variants in the SK2 channel gene (KCNN2) lead to dominant n..:
Mochel, Fanny
;
Rastetter, Agnès
;
Ceulemans, Berten
...
Brain. 143 (2020) 12 - p. 3564-3573 , 2020
Link:
https://doi.org/10.1093/..
?
4
The skeletal phenotype of intermediate GM1 gangliosidosis: ..:
Ferreira, Carlos R.
;
Regier, Debra S.
;
Yoon, Robin
...
Bone. 131 (2020) - p. 115142 , 2020
Link:
https://doi.org/10.1016/..
?
5
Prospective, phenotype-driven selection of critically ill n..:
Gubbels, Cynthia S.
;
VanNoy, Grace E.
;
Madden, Jill A.
...
Genetics in Medicine. 22 (2020) 4 - p. 736-744 , 2020
Link:
https://doi.org/10.1038/..
?
6
MN1 C-terminal truncation syndrome is a novel neurodevelopm..:
Mak, Christopher C Y
;
Doherty, Dan
;
Lin, Angela E
...
Brain. 143 (2019) 1 - p. 55-68 , 2019
Link:
https://doi.org/10.1093/..
?
7
Cost Optimization of Reverse Logistics : A Review:
, In:
Proceedings of the 7th International Conference on Information Communication and Management
,
Yang, Sandra
;
Taghipour, Atour
;
Canel-Depitre, Beatrice
- p. 158-161 , 2017
Link:
https://dl.acm.org/doi/1..
?
8
Racial and ethnic disparities in health care–associated Clo..:
Yang, Sandra
;
Rider, Briana B.
;
Baehr, Avi
..
American Journal of Infection Control. 44 (2016) 1 - p. 91-96 , 2016
Link:
https://doi.org/10.1016/..
?
9
Adverse Drug Event Prevention: 2014 Action Plan Conference:
Ducoffe, Aaron R.
;
Baehr, Avi
;
Peña, Juliet C.
...
American Journal of Medical Quality. 31 (2016) 5 - p. 476-485 , 2016
Link:
https://doi.org/10.1177/..
?
10
A novel mutation in the promoter of RARS2 causes pontocereb..:
Li, Zejuan
;
Schonberg, Rhonda
;
Guidugli, Lucia
...
Journal of Human Genetics. 60 (2015) 7 - p. 363-369 , 2015
Link:
https://doi.org/10.1038/..
?
11
MRI/MRS as a surrogate marker for clinical progression in G..:
Regier, Debra S.
;
Kwon, Hyuk Joon
;
Johnston, Jean
...
American Journal of Medical Genetics Part A. 170 (2015) 3 - p. 634-644 , 2015
Link:
https://doi.org/10.1002/..
?
12
Brain MRI in patients with GM1 gangliosidosis, type II: nov..:
Tifft, Cynthia J.
;
Kwon, H.J.
;
Regier, Debra S.
...
Molecular Genetics and Metabolism. 111 (2014) 2 - p. S103-S104 , 2014
Link:
https://doi.org/10.1016/..
?
13
Thiamine pyrophosphokinase deficiency causes a Leigh Diseas..:
Fraser, Jamie L.
;
Vanderver, Adeline
;
Yang, Sandra
...
Molecular Genetics and Metabolism Reports. 1 (2014) - p. 66-70 , 2014
Link:
https://doi.org/10.1016/..
?
14
The National Institutes of Health Undiagnosed Diseases Prog..:
Gahl, William A.
;
Markello, Thomas C.
;
Toro, Camilo
...
Genetics in Medicine. 14 (2012) 1 - p. 51-59 , 2012
Link:
https://doi.org/10.1038/..
?
15
Chitotriosidase as a Measure of Disease Burden in Patients ..:
Beattie, Lindsay
;
Yang, Sandra
;
Golas, Gretchen
...
Molecular Genetics and Metabolism. 105 (2012) 2 - p. S20 , 2012
Link:
https://doi.org/10.1016/..
1-15