E-LIB Suche - Ergebnisse für: Wallerstein, Robert

1

Complete uniparental disomy of chromosome 1 in a child with..:

Wallerstein, Violet ; Grant, Leon ; Wallerstein, Robert
Clinical Case Reports. 10 (2022) 7 - p. , 2022

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

2

Acute Rhabdomyolysis in a Child with Multiple Suspicious Ge..:

Murakami, Aiko ; Lau, Rhiana L. ; Wallerstein, Robert...
Case Reports in Pediatrics. 2022 (2022) - p. 1-5 , 2022

Link: https://doi.org/10.1155/..

3

Challenges in genetic counseling for congenital anomalies o..:

Gong, Ping ; Pelletier, Myriam ; Silverman, Neil..
Case Reports in Perinatal Medicine. 11 (2022) 1 - p. , 2022

Link: https://doi.org/10.1515/..

4

Mutations in IFT-A satellite core component genes IFT43 and..:

Duran, Ivan ; Taylor, S. Paige ; Zhang, Wenjuan...
Cilia. 6 (2017) 1 - p. , 2017

Link: https://doi.org/10.1186/..

5

Further Evidence That the CFTR Variant c.2620-6T>C Is Benig:

Wallerstein, Violet I. ; Wallerstein, Robert
Case Reports in Genetics. 2017 (2017) - p. 1-2 , 2017

Link: https://doi.org/10.1155/..

6

Deletion of 7q33-q35 in a Patient with Intellectual Disabil..:

Dilzell, Kristen ; Darcy, Diana ; Sum, John.
Case Reports in Genetics. 2015 (2015) - p. 1-5 , 2015

Link: https://doi.org/10.1155/..

7

Mosaic paternal genome‐wide uniparental isodisomy with down..:

Darcy, Diana ; Atwal, Paldeep Singh ; Angell, Cathy..
American Journal of Medical Genetics Part A. 167 (2015) 10 - p. 2463-2469 , 2015

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

8

Familial congenital bilateral vocal fold paralysis: A novel..:

Hsu, Amy K ; Rosow, David E. ; Wallerstein, Robert J..
International Journal of Pediatric Otorhinolaryngology. 79 (2015) 3 - p. 323-327 , 2015

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

9

Current knowledge of prenatal diagnosis of mosaic autosomal..:

Wallerstein, Robert ; Misra, Sonya ; Dugar, R. Bryce...
Prenatal Diagnosis. 35 (2015) 9 - p. 841-847 , 2015

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

10

Unusual Presentation of Pelizaeus-Merzbacher Disease: Femal..:

Brender, Teva ; Wallerstein, Donna ; Sum, John.
Case Reports in Genetics. 2015 (2015) - p. 1-3 , 2015

Link: https://doi.org/10.1155/..

11

A New Model for Providing Cell-Free DNA and Risk Assessment..:

Wallerstein, Robert ; Jelks, Andrea ; Garabedian, Matthew J.
Journal of Pregnancy. 2014 (2014) - p. 1-7 , 2014

Link: https://doi.org/10.1155/..

12

Genetic Variants for Long QT Syndrome among Infants and Chi..:

Chang, Ruey-Kang R. ; Lan, Yueh-Tze ; Silka, Michael J....
The Journal of Pediatrics. 164 (2014) 3 - p. 590-595.e3 , 2014

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

13

Antenatal detection of maternal unipartental disomy of chro..:

Quintana, Andrea ; Garabedian, Matthew J. ; Wallerstein, Robert J.
American Journal of Medical Genetics Part A. 164 (2013) 1 - p. 276-278 , 2013

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

14

Deletion of 3p25.3 in a patient with intellectual disabilit..:

Kellogg, Gregory ; Sum, John ; Wallerstein, Robert
American Journal of Medical Genetics Part A. 161 (2013) 6 - p. 1405-1408 , 2013

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

15

Long‐term survival with diaphanospondylodysostosis (DSD): S..:

Scottoline, Brian ; Rosenthal, Scott ; Keisari, Rami...
American Journal of Medical Genetics Part A. 158A (2012) 6 - p. 1447-1451 , 2012

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