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Chitayat, David
528
results:
Search for persons
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Format
Online (528)
Mediatypes
Articles (Online) (371)
Bookchapter (Online) (4)
OpenAccess-fulltext (153)
Sorted by: Year
Sorted by: Relevance
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1
P769: Trio-whole exome and whole genome sequencing in fetal..:
Gershon, Ariel
;
Anandampillai, Tanvi
;
Arshad, Maahil
...
Genetics in Medicine Open. 2 (2024) - p. 101677 , 2024
Link:
https://doi.org/10.1016/..
?
2
P812: Multiple fetal anomalies suggest a role for CDK20 in ..:
Chong, Karen
;
Chitayat, David
;
Ryan, Greg
...
Genetics in Medicine Open. 2 (2024) - p. 101720 , 2024
Link:
https://doi.org/10.1016/..
?
3
Associations and outcomes of prenatally detected rhombencep..:
Kunpalin, Yada
;
Miller, Elka
;
Raghuram, Kamini
...
Prenatal Diagnosis. , 2024
Link:
https://doi.org/10.1002/..
?
4
P866: Exploring the impact of secondary findings in a cohor..:
Fooks, Katharine
;
Vermeer, Lydia
;
Poole, Elise
...
Genetics in Medicine Open. 2 (2024) - p. 101780 , 2024
Link:
https://doi.org/10.1016/..
?
5
P610: Identification of trinucleotide repeat expansions in ..:
Guidugli, Lucia
;
Hammer, Monia
;
Cao, Bryant
...
Genetics in Medicine Open. 2 (2024) - p. 101516 , 2024
Link:
https://doi.org/10.1016/..
?
6
Validation of low‐pass genome sequencing for prenatal diagn..:
Mighton, Chloe
;
Noor, Abdul
;
Watkins, Nicholas
...
Prenatal Diagnosis. 44 (2024) 4 - p. 443-453 , 2024
Link:
https://doi.org/10.1002/..
?
7
Prenatal diagnosis of ROR‐2 related Robinow syndrome presen..:
Yang, Liying
;
Shannon, Patrick
;
Silver, Rachel
...
Prenatal Diagnosis. 44 (2024) 5 - p. 653-656 , 2024
Link:
https://doi.org/10.1002/..
?
8
P782: Validation of low-pass genome sequencing for prenatal..:
Mighton, Chloe
;
Noor, Abdul
;
Watkins, Nicholas
...
Genetics in Medicine Open. 2 (2024) - p. 101690 , 2024
Link:
https://doi.org/10.1016/..
?
9
P804: Prenatal diagnosis of atypical Holt-Oram syndrome cau..:
Mackley, Michael
;
Silver, Rachel
;
Watkins, Nicholas
...
Genetics in Medicine Open. 2 (2024) - p. 101712 , 2024
Link:
https://doi.org/10.1016/..
?
10
Revisiting the Implications of a Wide or Narrow Fetal Cavum..:
Sichitiu, Joanna
;
Ghannad‐Zadeh, Kimia
;
Van Mieghem, Tim
...
Journal of Ultrasound in Medicine. 43 (2024) 8 - p. 1461-1466 , 2024
Link:
https://doi.org/10.1002/..
?
11
P531: Developing the patient-reported Genetic testing Utili..:
Poole, Elise
;
Luca, Stephanie
;
Assamad, Daniel
...
Genetics in Medicine Open. 2 (2024) - p. 101430 , 2024
Link:
https://doi.org/10.1016/..
?
12
169 Curating the fetal genome: experience of the ClinGen pr..:
Galloway, Stephanie
;
Giordano, Jessica L.
;
Thomas-Wilson, Amanda
...
American Journal of Obstetrics and Gynecology. 230 (2024) 1 - p. S106 , 2024
Link:
https://doi.org/10.1016/..
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13
Expanding the phenotypic spectrum of NOTCH1 variants: clini..:
Stanley, Kaitlin J.
;
Kalbfleisch, Kelsey J.
;
Moran, Olivia M.
...
European Journal of Human Genetics. 32 (2024) 7 - p. 795-803 , 2024
Link:
https://doi.org/10.1038/..
?
14
A metabolic signature for NADSYN1-dependent congenital NAD ..:
Szot, Justin O.
;
Cuny, Hartmut
;
Martin, Ella M.M.A.
...
Journal of Clinical Investigation. 134 (2024) 4 - p. , 2024
Link:
https://doi.org/10.1172/..
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15
Heart transplantation in neonatal Marfan syndrome: Saving l..:
Laks, Jessica A.
;
Lynch, Aine
;
Honjo, Osami
...
Pediatric Transplantation. 27 (2023) 6 - p. , 2023
Link:
https://doi.org/10.1111/..
1-15