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American Journal of Medical Genetics
|
September 20, 2000
Mutation analysis and description of sixteen RSH/Smith-Lemli-Opitz syndrome patients: polymerase chain reaction-based assays to simplify genotyping
P A Krakowiak, N A Nwokoro, C A Wassif, et al.
American Journal of Human Genetics
|
June 9, 2009
Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations
Paweł Stankiewicz, Partha Sen, Samarth S Bhatt, et al.
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Showing results (31-40 of 32) with videos related to
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Page
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You have reached the last page of results.
This site can display upto 32 results.
American Journal of Medical Genetics
|
September 20, 2000
Mutation analysis and description of sixteen RSH/Smith-Lemli-Opitz syndrome patients: polymerase chain reaction-based assays to simplify genotyping
P A Krakowiak, N A Nwokoro, C A Wassif, et al.
American Journal of Human Genetics
|
June 9, 2009
Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations
Paweł Stankiewicz, Partha Sen, Samarth S Bhatt, et al.
Page
of 4