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Clinical Genetics
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April 17, 2013
'Deletion rescue' by mitotic 11q uniparental disomy in a family with recurrence of 11q deletion Jacobsen syndrome
J P Johnson, M Haag, L Beischel, et al.
American Journal of Medical Genetics. Part A
|
May 16, 2003
Genetic and clinical characterization of patients with an interstitial duplication 15q11-q13, emphasizing behavioral phenotype and response to treatment
J A Thomas, J Johnson, T L Peterson Kraai, et al.
Molecular Genetics and Metabolism
|
May 15, 2001
Hepatic carnitine palmitoyl transferase 1 (CPT1 A) deficiency in North American Hutterites (Canadian and American): evidence for a founder effect and results of a pilot study on a DNA-based newborn screening program
C Prasad, J P Johnson, J P Bonnefont, 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.
Clinical Genetics
|
April 17, 2013
'Deletion rescue' by mitotic 11q uniparental disomy in a family with recurrence of 11q deletion Jacobsen syndrome
J P Johnson, M Haag, L Beischel, et al.
American Journal of Medical Genetics. Part A
|
May 16, 2003
Genetic and clinical characterization of patients with an interstitial duplication 15q11-q13, emphasizing behavioral phenotype and response to treatment
J A Thomas, J Johnson, T L Peterson Kraai, et al.
Molecular Genetics and Metabolism
|
May 15, 2001
Hepatic carnitine palmitoyl transferase 1 (CPT1 A) deficiency in North American Hutterites (Canadian and American): evidence for a founder effect and results of a pilot study on a DNA-based newborn screening program
C Prasad, J P Johnson, J P Bonnefont, et al.
Page
of 2