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Jakielski, Kathy J.
33
results:
Online X
Format
Online (33)
Mediatypes
Articles (Online) (7)
OpenAccess-fulltext (26)
Sorted by: Relevance
Sorted by: Year
?
1
A single case experimental design study using an operationa..:
Gomez, Maryane
;
Purcell, Alison
;
Jakielski, Kathy
.
International Journal of Speech-Language Pathology. 26 (2023) 2 - p. 194-211 , 2023
Link:
https://doi.org/10.1080/..
?
2
Estimates of the prevalence of speech and motor speech diso..:
Shriberg, Lawrence D.
;
Strand, Edythe A.
;
Jakielski, Kathy J.
.
Clinical Linguistics & Phonetics. 33 (2019) 8 - p. 707-736 , 2019
Link:
https://doi.org/10.1080/..
?
3
A set of regulatory genes co-expressed in embryonic human b..:
Eising, Else
;
Carrion-Castillo, Amaia
;
Vino, Arianna
...
Molecular Psychiatry. 24 (2018) 7 - p. 1065-1078 , 2018
Link:
https://doi.org/10.1038/..
?
4
Whole-exome sequencing supports genetic heterogeneity in ch..:
Worthey, Elizabeth A
;
Raca, Gordana
;
Laffin, Jennifer J
...
Journal of Neurodevelopmental Disorders. 5 (2013) 1 - p. , 2013
Link:
https://doi.org/10.1186/..
?
5
Novel candidate genes and regions for childhood apraxia of ..:
Laffin, Jennifer J.S.
;
Raca, Gordana
;
Jackson, Craig A.
...
Genetics in Medicine. 14 (2012) 11 - p. 928-936 , 2012
Link:
https://doi.org/10.1038/..
?
6
Phenotype of FOXP2 haploinsufficiency in a mother and son:
Rice, Gregory M.
;
Raca, Gordana
;
Jakielski, Kathy J.
...
American Journal of Medical Genetics Part A. 158A (2011) 1 - p. 174-181 , 2011
Link:
https://doi.org/10.1002/..
?
7
Breakpoint localization using array‐CGH in three siblings w..:
Shriberg, Lawrence D.
;
Jakielski, Kathy J.
;
El‐Shanti, Hatem
American Journal of Medical Genetics Part A. 146A (2008) 17 - p. 2227-2233 , 2008
Link:
https://doi.org/10.1002/..
?
8
Author Correction: CHD3 helicase domain mutations cause a n..:
Snijders Blok, Lot
;
Rousseau, Justine
;
Twist, Joanna
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497626/. , 2019
Link:
http://www.ncbi.nlm.nih...
?
9
Estimates of the prevalence of speech and motor speech diso..:
Shriberg, Lawrence D
;
Strand, Edythe A
;
Jakielski, Kathy J
.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6633911/. , 2019
Link:
http://www.ncbi.nlm.nih...
?
10
Author Correction: CHD3 helicase domain mutations cause a n..:
Blok, Lot Snijders
;
Rousseau, Justine
;
Twist, Joanna
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6377600/. , 2019
Link:
http://www.ncbi.nlm.nih...
?
11
CHD3 helicase domain mutations cause a neurodevelopmental s..:
Snijders Blok, Lot
;
Rousseau, Justine
;
Twist, Joanna
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41467-018-06014-6. , 2018
Link:
https://hal.sorbonne-uni..
?
12
CHD3 helicase domain mutations cause a neurodevelopmental s..:
Snijders Blok, Lot
;
Rousseau, Justine
;
Twist, Joanna
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218476/. , 2018
Link:
http://www.ncbi.nlm.nih...
?
13
A set of regulatory genes co-expressed in embryonic human b..:
Eising, Else
;
Carrion-Castillo, Amaia
;
Vino, Arianna
...
hal-01726218. , 2018
Link:
https://hal.archives-ouv..
?
14
CHD3 helicase domain mutations cause a neurodevelopmental s..:
Blok, Lot Snijders
;
Rousseau, Justine
;
Twist, Joanna
...
2041-1723. , 2018
Link:
https://dspace.library.u..
?
15
A set of regulatory genes co-expressed in embryonic human b..:
Eising, Else
;
Carrion-Castillo, Amaia
;
Vino, Arianna
...
hal-01726218. , 2018
Link:
https://hal.science/hal-..
1-15