E-LIB Suche - Ergebnisse für: Curtis Rogers

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

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/..

9

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/..

10

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/..

11

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/..

12

The vectoring competence of the mite Varroa destructor for ..:

Ryabov, Eugene V. ; Posada-Florez, Francisco ; Rogers, Curtis...
Frontiers in Insect Science. 2 (2022) - p. , 2022

Link: https://doi.org/10.3389/..

13

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/..

14

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/..

15

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/..