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American Journal of Human Genetics
|
June 23, 1998
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis
K Buiting, B Dittrich, S Gross, et al.
Neurology
|
August 1, 2007
Location and type of mutation in the LIS1 gene do not predict phenotypic severity
G Uyanik, D J Morris-Rosendahl, J Stiegler, et al.
American Journal of Human Genetics
|
December 12, 2000
Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and III
H J Lüdecke, J Schaper, P Meinecke, et al.
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Search research articles
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Showing results (91-100 of 93) with videos related to
Sort By:
Page
of 10
You have reached the last page of results.
This site can display upto 93 results.
American Journal of Human Genetics
|
June 23, 1998
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis
K Buiting, B Dittrich, S Gross, et al.
Neurology
|
August 1, 2007
Location and type of mutation in the LIS1 gene do not predict phenotypic severity
G Uyanik, D J Morris-Rosendahl, J Stiegler, et al.
American Journal of Human Genetics
|
December 12, 2000
Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and III
H J Lüdecke, J Schaper, P Meinecke, et al.
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of 10