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American Journal of Medical Genetics
|
March 1, 1994
Hypoplasia of the cerebellar vermis and corpus callosum in thrombocytopenia with absent radius syndrome on MRI studies
M R MacDonald, G B Schaefer, A H Olney, et al.
The Nebraska Medical Journal
|
March 1, 1986
The twenty-five most common multiple congenital anomaly syndromes in Nebraska
P L Jacobsen, A H Olney, W G Sanger, et al.
American Journal of Medical Genetics
|
July 1, 1993
Brain magnetic resonance imaging findings in the Opitz G/BBB syndrome: extension of the spectrum of midline brain anomalies
M R MacDonald, G B Schaefer, A H Olney, et al.
AJNR. American Journal of Neuroradiology
|
December 24, 2011
Novel proximal 14q deletion: clinical and diffusion tensor imaging tractography findings in a patient with lissencephaly, agenesis of the corpus callosum, and septo-optic dysplasia
E K Bravo, M L White, A H Olney, et al.
Genomics
|
January 1, 1989
Mapping of the human complement factor I gene to 4q25
R Shiang, J C Murray, C C Morton, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
April 13, 2025
The distinctive P450 oxidoreductase (PORD) urinary steroid metabolome in the first week of life: Report of three cases with severe disorder
E S Baranowski, J Idkowiak, J Waterson, et al.
American Journal of Medical Genetics
|
October 2, 1996
Report from the workshop on Pallister-Hall syndrome and related phenotypes
L G Biesecker, M Abbott, J Allen, et al.
Journal of Dental Research
|
June 16, 2012
Dental abnormalities in Schimke immuno-osseous dysplasia
M Morimoto, O Kérourédan, M Gendronneau, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 28 results.
American Journal of Medical Genetics
|
March 1, 1994
Hypoplasia of the cerebellar vermis and corpus callosum in thrombocytopenia with absent radius syndrome on MRI studies
M R MacDonald, G B Schaefer, A H Olney, et al.
The Nebraska Medical Journal
|
March 1, 1986
The twenty-five most common multiple congenital anomaly syndromes in Nebraska
P L Jacobsen, A H Olney, W G Sanger, et al.
American Journal of Medical Genetics
|
July 1, 1993
Brain magnetic resonance imaging findings in the Opitz G/BBB syndrome: extension of the spectrum of midline brain anomalies
M R MacDonald, G B Schaefer, A H Olney, et al.
AJNR. American Journal of Neuroradiology
|
December 24, 2011
Novel proximal 14q deletion: clinical and diffusion tensor imaging tractography findings in a patient with lissencephaly, agenesis of the corpus callosum, and septo-optic dysplasia
E K Bravo, M L White, A H Olney, et al.
Genomics
|
January 1, 1989
Mapping of the human complement factor I gene to 4q25
R Shiang, J C Murray, C C Morton, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
April 13, 2025
The distinctive P450 oxidoreductase (PORD) urinary steroid metabolome in the first week of life: Report of three cases with severe disorder
E S Baranowski, J Idkowiak, J Waterson, et al.
American Journal of Medical Genetics
|
October 2, 1996
Report from the workshop on Pallister-Hall syndrome and related phenotypes
L G Biesecker, M Abbott, J Allen, et al.
Journal of Dental Research
|
June 16, 2012
Dental abnormalities in Schimke immuno-osseous dysplasia
M Morimoto, O Kérourédan, M Gendronneau, et al.
Page
of 3