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G M Cooper

Showing results (201-210 of 205) with videos related to

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The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|June 20, 2015
Transforming Growth Factor-β3 Therapy Delays Postoperative Reossification and Improves Craniofacial Growth in Craniosynostotic RabbitsJ Gilbert, M Karski, T D Smith, et al.
The Journal of Craniofacial Surgery|July 1, 1999
Coronal suture response to distraction osteogenesis in rabbits with delayed-onset craniosynostosisH W Losken, M P Mooney, J Zoldos, et al.
Journal of Medical Genetics|June 14, 2008
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variantF D Hannes, A J Sharp, H C Mefford, et al.
Clinical Genetics|April 14, 2018
Systematic reanalysis of genomic data improves quality of variant interpretationS M Hiatt, M D Amaral, K M Bowling, et al.
Nature|April 25, 2014
Guidelines for investigating causality of sequence variants in human diseaseD G MacArthur, T A Manolio, D P Dimmock, et al.
Pageof 21

Showing results (201-210 of 205) with videos related to

Sort By:
Pageof 21
You have reached the last page of results.This site can display upto 205 results.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|June 20, 2015
Transforming Growth Factor-β3 Therapy Delays Postoperative Reossification and Improves Craniofacial Growth in Craniosynostotic RabbitsJ Gilbert, M Karski, T D Smith, et al.
The Journal of Craniofacial Surgery|July 1, 1999
Coronal suture response to distraction osteogenesis in rabbits with delayed-onset craniosynostosisH W Losken, M P Mooney, J Zoldos, et al.
Journal of Medical Genetics|June 14, 2008
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variantF D Hannes, A J Sharp, H C Mefford, et al.
Clinical Genetics|April 14, 2018
Systematic reanalysis of genomic data improves quality of variant interpretationS M Hiatt, M D Amaral, K M Bowling, et al.
Nature|April 25, 2014
Guidelines for investigating causality of sequence variants in human diseaseD G MacArthur, T A Manolio, D P Dimmock, et al.
Pageof 21