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Curtis Rogers
354
results:
english X
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Format
Online (354)
Mediatypes
E-Books (6)
Articles (Online) (178)
Bookchapter (Online) (1)
OpenAccess-fulltext (169)
Sorted by: Relevance
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?
1
Prenatal diagnosis of mosaicism for deletion 22q13.3:
Phelan, Mary C.
;
Brown, Elizabeth F.
;
Curtis Rogers, R.
Prenatal Diagnosis. 21 (2001) 12 - p. 1100-1100 , 2001
Link:
https://doi.org/10.1002/..
?
2
Prenatal diagnosis of mosaicism for triploidy and trisomy 1:
Phelan, Mary C.
;
Curtis Rogers, R.
;
Michaelis, Ron C.
..
Prenatal Diagnosis. 21 (2001) 6 - p. 457-460 , 2001
Link:
https://doi.org/10.1002/..
?
3
Germline mosaicism in X‐linked myotubular myopathy:
Häne, Bernhard G
;
Curtis Rogers, R
;
Schwartz, Charles E
Clinical Genetics. 56 (1999) 1 - p. 77-81 , 1999
Link:
https://doi.org/10.1034/..
?
4
P163: Functional assessment of IGF-1 and hGH as candidate t..:
Moffitt, Bridgette
;
Spencer, Jillian
;
Benjock, Jennifer
...
Genetics in Medicine Open. 2 (2024) - p. 101060 , 2024
Link:
https://doi.org/10.1016/..
?
5
Head Size in Phelan–McDermid Syndrome: A Literature Review ..:
Sarasua, Sara M.
;
DeLuca, Jane M.
;
Rogers, Curtis
...
Genes. 14 (2023) 3 - p. 540 , 2023
Link:
https://doi.org/10.3390/..
?
6
Stratification of a Phelan–McDermid Syndrome Population Bas..:
Moffitt, Bridgette A.
;
Sarasua, Sara M.
;
Ivankovic, Diana
...
Genes. 14 (2023) 2 - p. 490 , 2023
Link:
https://doi.org/10.3390/..
?
7
Lymphedema is associated with CELSR1 in Phelan–McDermid syn..:
Smith, Marie S.
;
Sarasua, Sara M.
;
Rogers, Curtis
..
Clinical Genetics. 104 (2023) 4 - p. 472-478 , 2023
Link:
https://doi.org/10.1111/..
?
8
Phenotypic Variability in Phelan–McDermid Syndrome and Its ..:
Boccuto, Luigi
;
Mitz, Andrew
;
Abenavoli, Ludovico
...
Genes. 13 (2022) 3 - p. 528 , 2022
Link:
https://doi.org/10.3390/..
?
9
FC044: Heterozygous Variants in Kinase Domain of NEK8 cause..:
Claus, Laura
;
Stallworth, Jennifer
;
van Jaarsveld, Richard
...
Nephrology Dialysis Transplantation. 37 (2022) Supplement_3 - p. , 2022
Link:
https://doi.org/10.1093/..
?
10
eP413: Type II cat eye syndrome in a newborn with intrauter..:
Wang, Jiyong
;
Waters, Marsha
;
Witt, Loretta
...
Genetics in Medicine. 24 (2022) 3 - p. S259 , 2022
Link:
https://doi.org/10.1016/..
?
11
RNA analysis of the GALNS transcript reveals novel pathogen..:
Sohn, Young Bae
;
Rogers, Curtis
;
Stallworth, Jennifer
...
Molecular Genetics and Metabolism Reports. 31 (2022) - p. 100875 , 2022
Link:
https://doi.org/10.1016/..
?
12
OP047: Timely diagnosis of mucopolysaccharidosis: Results f..:
Yu, Christine
;
Clarke, Lorne
;
Rogers, Curtis
Genetics in Medicine. 24 (2022) 3 - p. S371-S372 , 2022
Link:
https://doi.org/10.1016/..
?
13
Sleep and Phelan–McDermid Syndrome: Lessons from the Intern..:
Moffitt, Bridgette A.
;
Sarasua, Sara M.
;
Ward, Linda
...
Molecular Genetics & Genomic Medicine. 10 (2022) 10 - p. , 2022
Link:
https://doi.org/10.1002/..
?
14
Position effects of 22q13 rearrangements on candidate genes..:
Srikanth, Sujata
;
Jain, Lavanya
;
Zepeda-Mendoza, Cinthya
...
PLOS ONE. 16 (2021) 7 - p. e0253859 , 2021
Link:
https://doi.org/10.1371/..
?
15
1q21.1 deletion size and associated clinical presentations:
Wang, Jiyong
;
Hamid, Rasikh
;
Lyons, Michael
...
Molecular Genetics and Metabolism. 132 (2021) - p. S241-S243 , 2021
Link:
https://doi.org/10.1016/..
1-15