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Prenatal Diagnosis
|
January 8, 2014
A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes
J Besseau-Ayasse, C Violle-Poirsier, A Bazin, et al.
Neurogenetics
|
March 8, 2018
MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype
T Smol, F Petit, A Piton, et al.
Nature
|
February 5, 2010
A new highly penetrant form of obesity due to deletions on chromosome 16p11.2
R G Walters, S Jacquemont, A Valsesia, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 13) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 13 results.
Prenatal Diagnosis
|
January 8, 2014
A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes
J Besseau-Ayasse, C Violle-Poirsier, A Bazin, et al.
Neurogenetics
|
March 8, 2018
MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype
T Smol, F Petit, A Piton, et al.
Nature
|
February 5, 2010
A new highly penetrant form of obesity due to deletions on chromosome 16p11.2
R G Walters, S Jacquemont, A Valsesia, et al.
Page
of 2