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Steven A Wall

Showing results (41-50 of 72) with videos related to

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Journal of Neurosurgery. Pediatrics|August 13, 2021
Clinical signs, interventions, and treatment course of three different treatment protocols in patients with Crouzon syndrome with acanthosis nigricansCatherine A de Planque, Steven A Wall, Louise Dalton, et al.
Pediatrics|July 21, 2010
Prevalence and complications of single-gene and chromosomal disorders in craniosynostosisAndrew O M Wilkie, Jo C Byren, Jane A Hurst, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|March 11, 2006
Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patientsFernanda Sarquis Jehee, Luis G Alonso, Denise P Cavalcanti, et al.
BMC Medical Genetics|September 2, 2014
Apparently synonymous substitutions in FGFR2 affect splicing and result in mild Crouzon syndromeAimee L Fenwick, Jacqueline A C Goos, Julia Rankin, et al.
American Journal of Medical Genetics. Part A|July 14, 2006
Clinical dividends from the molecular genetic diagnosis of craniosynostosisAndrew O M Wilkie, Elena G Bochukova, Ruth M S Hansen, et al.
American Journal of Medical Genetics. Part A|July 11, 2007
Clinical dividends from the molecular genetic diagnosis of craniosynostosisAndrew O M Wilkie, Elena G Bochukova, Ruth M S Hansen, et al.
American Journal of Human Genetics|January 10, 2002
Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosisShih-hsin Kan, Navaratnam Elanko, David Johnson, et al.
Journal of Medical Genetics|September 18, 2014
De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorderChristian Babbs, Deborah Lloyd, Alistair T Pagnamenta, et al.
Journal of Anatomy|May 17, 2024
Reassessing the association: Evaluation of a polyalanine deletion variant of RUNX2 in non-syndromic sagittal and metopic craniosynostosisIsaac S Walton, Emma McCann, Astrid Weber, et al.
Journal of Medical Genetics|January 13, 2021
Unexpected role of <i>SIX1</i> variants in craniosynostosis: expanding the phenotype of <i>SIX1</i>-related disordersEduardo Calpena, Maud Wurmser, Simon J McGowan, et al.
Pageof 8

Showing results (41-50 of 72) with videos related to

Sort By:
Pageof 8
Journal of Neurosurgery. Pediatrics|August 13, 2021
Clinical signs, interventions, and treatment course of three different treatment protocols in patients with Crouzon syndrome with acanthosis nigricansCatherine A de Planque, Steven A Wall, Louise Dalton, et al.
Pediatrics|July 21, 2010
Prevalence and complications of single-gene and chromosomal disorders in craniosynostosisAndrew O M Wilkie, Jo C Byren, Jane A Hurst, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|March 11, 2006
Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patientsFernanda Sarquis Jehee, Luis G Alonso, Denise P Cavalcanti, et al.
BMC Medical Genetics|September 2, 2014
Apparently synonymous substitutions in FGFR2 affect splicing and result in mild Crouzon syndromeAimee L Fenwick, Jacqueline A C Goos, Julia Rankin, et al.
American Journal of Medical Genetics. Part A|July 14, 2006
Clinical dividends from the molecular genetic diagnosis of craniosynostosisAndrew O M Wilkie, Elena G Bochukova, Ruth M S Hansen, et al.
American Journal of Medical Genetics. Part A|July 11, 2007
Clinical dividends from the molecular genetic diagnosis of craniosynostosisAndrew O M Wilkie, Elena G Bochukova, Ruth M S Hansen, et al.
American Journal of Human Genetics|January 10, 2002
Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosisShih-hsin Kan, Navaratnam Elanko, David Johnson, et al.
Journal of Medical Genetics|September 18, 2014
De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorderChristian Babbs, Deborah Lloyd, Alistair T Pagnamenta, et al.
Journal of Anatomy|May 17, 2024
Reassessing the association: Evaluation of a polyalanine deletion variant of RUNX2 in non-syndromic sagittal and metopic craniosynostosisIsaac S Walton, Emma McCann, Astrid Weber, et al.
Journal of Medical Genetics|January 13, 2021
Unexpected role of <i>SIX1</i> variants in craniosynostosis: expanding the phenotype of <i>SIX1</i>-related disordersEduardo Calpena, Maud Wurmser, Simon J McGowan, et al.
Pageof 8