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Emma L Wakeling

Showing results (1-10 of 33) with videos related to

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Archives of Disease in Childhood|February 26, 2011
Silver-Russell syndromeEmma L Wakeling
Clinical Dysmorphology|April 5, 2008
Congenital microgastria in association with Pierre-Robin sequenceDaniel E Laurie, Emma L Wakeling
Clinical Dysmorphology|December 13, 2006
Aplasia cutis congenita, terminal limb defects and falciform retinal folds: confirmation of a distinct syndrome of vascular disruptionJoanna Prothero, Richard Nicholl, Judith Wilson, et al.
Clinical Dysmorphology|February 2, 2002
X-linked inheritance of Dandy-Walker variantEmma L Wakeling, Matthew Jolly, Nicholas M Fisk, et al.
Clinical Dysmorphology|December 3, 2009
A distinct autosomal recessive disorder of limb development with preaxial brachydactyly, phalangeal duplication, symphalangism and hyperphalangismHermione Race, Christine M Hall, Mike G Harrison, et al.
Clinical Dysmorphology|July 19, 2003
Septo-optic dysplasia, subglottic stenosis and skeletal abnormalities: a case reportEmma L Wakeling, Mehul T Dattani, A Bloch-Zupan, et al.
Pediatric Radiology|May 19, 2004
Central osteosclerosis with trichothiodystrophyEmma L Wakeling, Michele Cruwys, Mohnish Suri, et al.
Journal of Medical Genetics|March 23, 2010
Epigenetic signatures of Silver-Russell syndromeSayeda Abu-Amero, Emma L Wakeling, Mike Preece, et al.
Journal of Dermatological Science|September 28, 2011
Exacerbation of X-linked ichthyosis phenotype in a female by inheritance of filaggrin and steroid sulfatase mutationsRaakhee Ramesh, Huijia Chen, Anna Kukula, et al.
Journal of Medical Genetics|December 21, 2022
Craniosynostosis, inner ear, and renal anomalies in a child with complete loss of <i>SPRY1</i> (sprouty homolog 1) functionRebecca S Tooze, Eduardo Calpena, Stephen R F Twigg, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Archives of Disease in Childhood|February 26, 2011
Silver-Russell syndromeEmma L Wakeling
Clinical Dysmorphology|April 5, 2008
Congenital microgastria in association with Pierre-Robin sequenceDaniel E Laurie, Emma L Wakeling
Clinical Dysmorphology|December 13, 2006
Aplasia cutis congenita, terminal limb defects and falciform retinal folds: confirmation of a distinct syndrome of vascular disruptionJoanna Prothero, Richard Nicholl, Judith Wilson, et al.
Clinical Dysmorphology|February 2, 2002
X-linked inheritance of Dandy-Walker variantEmma L Wakeling, Matthew Jolly, Nicholas M Fisk, et al.
Clinical Dysmorphology|December 3, 2009
A distinct autosomal recessive disorder of limb development with preaxial brachydactyly, phalangeal duplication, symphalangism and hyperphalangismHermione Race, Christine M Hall, Mike G Harrison, et al.
Clinical Dysmorphology|July 19, 2003
Septo-optic dysplasia, subglottic stenosis and skeletal abnormalities: a case reportEmma L Wakeling, Mehul T Dattani, A Bloch-Zupan, et al.
Pediatric Radiology|May 19, 2004
Central osteosclerosis with trichothiodystrophyEmma L Wakeling, Michele Cruwys, Mohnish Suri, et al.
Journal of Medical Genetics|March 23, 2010
Epigenetic signatures of Silver-Russell syndromeSayeda Abu-Amero, Emma L Wakeling, Mike Preece, et al.
Journal of Dermatological Science|September 28, 2011
Exacerbation of X-linked ichthyosis phenotype in a female by inheritance of filaggrin and steroid sulfatase mutationsRaakhee Ramesh, Huijia Chen, Anna Kukula, et al.
Journal of Medical Genetics|December 21, 2022
Craniosynostosis, inner ear, and renal anomalies in a child with complete loss of <i>SPRY1</i> (sprouty homolog 1) functionRebecca S Tooze, Eduardo Calpena, Stephen R F Twigg, et al.
Pageof 4