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Crowe, Carol
129
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Online (129)
Mediatypes
E-Books (1)
Articles (Online) (83)
Bookchapter (Online) (5)
OpenAccess-fulltext (40)
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1
Left Ventricular Dysfunction in Duchenne Muscular Dystrophy..:
Ashwath, Mahi L.
;
Jacobs, Irwin B.
;
Crowe, Carol A.
...
The American Journal of Cardiology. 114 (2014) 2 - p. 284-289 , 2014
Link:
https://doi.org/10.1016/..
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2
Genetic dysfunction ofMT-ATP6causes axonal Charcot-Marie-To..:
Pitceathly, Robert D.S.
;
Murphy, Sinéad M.
;
Cottenie, Ellen
...
Neurology. 79 (2012) 11 - p. 1145-1154 , 2012
Link:
https://doi.org/10.1212/..
?
3
Germline mosaicism in Cornelia de Lange syndrome:
Slavin, Thomas P.
;
Lazebnik, Noam
;
Clark, Dinah M.
...
American Journal of Medical Genetics Part A. 158A (2012) 6 - p. 1481-1485 , 2012
Link:
https://doi.org/10.1002/..
?
4
Duplication of the pituitary gland associated with multiple..:
Geertman, RobertT
;
Manjila, Sunil
;
Vadera, Sumeet
...
Surgical Neurology International. 3 (2012) 1 - p. 23 , 2012
Link:
https://doi.org/10.4103/..
?
5
Novel LMNA mutations in patients with Emery-Dreifuss muscul..:
Scharner, Juergen
;
Brown, Charlotte A.
;
Bower, Matthew
...
Human Mutation. 32 (2011) 2 - p. 152-167 , 2011
Link:
https://doi.org/10.1002/..
?
6
Cardiac and Pulmonary Function Variability in Duchenne/Beck..:
Birnkrant, David J.
;
Ashwath, Mahi Lakshmi
;
Noritz, Garey H.
...
Journal of Child Neurology. 25 (2010) 9 - p. 1110-1115 , 2010
Link:
https://doi.org/10.1177/..
?
7
Regional genomic instability predisposes to complex dystrop..:
Oshima, Junko
;
Magner, Daniel B.
;
Lee, Jennifer A.
...
Human Genetics. 126 (2009) 3 - p. 411-423 , 2009
Link:
https://doi.org/10.1007/..
?
8
Clinical and Genetic Features in Two Families With MELAS an..:
Tay, Stacey K. H.
;
Shanske, Sara
;
Crowe, Carol
...
Journal of Child Neurology. 20 (2005) 2 - p. 142-146 , 2005
Link:
https://doi.org/10.1177/..
?
9
Brown syndrome associated with velocardiofacial syndrome:
Chang, Susie
;
Crowe, Carol A
;
Traboulsi, Elias I
Journal of American Association for Pediatric Ophthalmology and Strabismus. 8 (2004) 3 - p. 290-292 , 2004
Link:
https://doi.org/10.1016/..
?
10
Characterization of GATA3 Mutations in the Hypoparathyroidi..:
Nesbit, M. Andrew
;
Bowl, Michael R.
;
Harding, Brian
...
Journal of Biological Chemistry. 279 (2004) 21 - p. 22624-22634 , 2004
Link:
https://doi.org/10.1074/..
?
11
Congenital hypomyelinating neuropathy, central dysmyelinati..:
Inoue, Ken
;
Shilo, Konstantin
;
Boerkoel, Cornelius F.
...
Annals of Neurology. 52 (2002) 6 - p. 836-842 , 2002
Link:
https://doi.org/10.1002/..
?
12
Novel and recurrent mutations in lamin A/C in patients with..:
Brown, Charlotte A.
;
Lanning, Robert W.
;
McKinney, Kimberly Q.
...
American Journal of Medical Genetics. 102 (2001) 4 - p. 359-367 , 2001
Link:
https://doi.org/10.1002/..
?
13
Book Review: A Comprehensive Primer on Medical Genetics:
Crowe, Carol
Clinical Pediatrics. 39 (2000) 1 - p. 59-59 , 2000
Link:
https://doi.org/10.1177/..
?
14
Risk of abnormal pregnancy outcome in carriers of balanced ..:
Pollin, Toni I.
;
Dobyns, William B.
;
Crowe, Carol A.
...
American Journal of Medical Genetics. 85 (1999) 4 - p. 369-375 , 1999
Link:
https://doi.org/10.1002/..
?
15
Mosaic trisomy 22: A case presentation and literature revie..:
Crowe, Carol A.
;
Schwartz, Stuart
;
Black, Cynthia J.
.
American Journal of Medical Genetics. 71 (1997) 4 - p. 406-413 , 1997
Link:
https://doi.org/10.1002/..
1-15