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Clinical Dysmorphology|December 17, 2004
Mutation analysis of TBX22 reveals new mutation in Tunisian CPX familyMyriam Chaabouni, Nizar Smaoui, Neila Benneji, et al.
Clinical Dysmorphology|December 17, 2004
Familial megalencephaly with dilated Virchow-Robin spaces in magnetic resonance imaging: an autosomal recessive trait?Christoph Härtel, Sandra Bachmann, Carsten Bönnemann, et al.
Clinical Dysmorphology|December 17, 2004
Isochromosome 20p associated with multiple congenital abnormalitiesAlan E Fryer, Michael Ashworth, Jed Hawe, et al.
Clinical Dysmorphology|December 17, 2004
Survival up to age 10 years in a patient with partial duplication 6q: case report and review of the literatureCornelia Seel, Hans-Dieter Hager, Anna Jauch, et al.
Clinical Dysmorphology|March 17, 2005
Further delineation of the 22q13 deletion syndromeS G Lindquist, M Kirchhoff, C Lundsteen, et al.
Clinical Dysmorphology|March 17, 2005
Exclusion of TCOF1 mutations in a case of bilateral Goldenhar syndrome and one familial case of microtia with meatal atresiaChristian T Thiel, Frank Rosanowski, Jürgen Kohlhase, et al.
Clinical Dysmorphology|March 17, 2005
Severe feeding difficulties in 3C syndromePrasad Iyer, Rupert Smith
Clinical Dysmorphology|April 5, 2008
De Barsy syndrome: a review of the phenotypeEmma C Kivuva, Michael J Parker, Marta C Cohen, et al.
Clinical Dysmorphology|April 5, 2008
The fifth female patient with Myhre syndrome: further delineationLuis E Becerra-Solano, Manuel Díaz-Rodriguez, Jose A Nastasi-Catanese, et al.
Clinical Dysmorphology|November 21, 1998
Acro-renal-ocular syndrome: expansion of the phenotypeE Guillén-Navarro, R Wallerstein, E Reich, et al.
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