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European Journal of Human Genetics : EJHG
|
February 15, 2001
Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia
N Matsumoto, R J Leventer, J A Kuc, et al.
Human Molecular Genetics
|
December 15, 2000
The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 gene
C Cardoso, R J Leventer, N Matsumoto, et al.
European Journal of Medical Genetics
|
July 8, 2022
Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory services
C A Stutterd, A Vanderver, P J Lockhart, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
May 4, 2021
Prenatal diagnosis of rhombencephalosynapsis: neuroimaging features and severity of vermian anomaly
K Krajden Haratz, P Oliveira Szejnfeld, M Govindaswamy, et al.
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of 3
Search research articles
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Showing results (21-30 of 24) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 24 results.
European Journal of Human Genetics : EJHG
|
February 15, 2001
Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia
N Matsumoto, R J Leventer, J A Kuc, et al.
Human Molecular Genetics
|
December 15, 2000
The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 gene
C Cardoso, R J Leventer, N Matsumoto, et al.
European Journal of Medical Genetics
|
July 8, 2022
Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory services
C A Stutterd, A Vanderver, P J Lockhart, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
May 4, 2021
Prenatal diagnosis of rhombencephalosynapsis: neuroimaging features and severity of vermian anomaly
K Krajden Haratz, P Oliveira Szejnfeld, M Govindaswamy, et al.
Page
of 3