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Genetic Counseling (Geneva, Switzerland)|May 25, 2006
Waardenburg syndrome in the Turkish deaf populationF Silan, C Zafer, I OnderGenetic Counseling (Geneva, Switzerland)|May 25, 2006
Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter)C P Chen, S P Lin, C C Lin, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1997
A new type of maxillofacial dysostosis, inherited as an X-linked or autosomal recessive traitR J Ensink, H G Brunner, C W CremersGenetic Counseling (Geneva, Switzerland)|April 29, 1998
Neonatal death in Marshall-Smith syndromeC Chatel, F Maazoul, S Sigaudy, et al.Genetic Counseling (Geneva, Switzerland)|April 29, 1998
Lymphedema combined with brachydactyly and tachycardiaC Stoll, Y Alembik, B Dott, et al.Genetic Counseling (Geneva, Switzerland)|January 22, 2005
Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosomeM G E M Ausems, J Schuil, C Van Raveswaaij-Arts, et al.Genetic Counseling (Geneva, Switzerland)|January 22, 2005
Trisomy 1q43 syndrome: a consistent phenotype with macrocephaly, characteristic face, developmental delay and cardiac anomaliesE Morava, K E Jackson, F Tsien, et al.Genetic Counseling (Geneva, Switzerland)|January 22, 2005
Complex facio-audio-symphalangism syndrome. An autosomal recessive type?S Balci, I YigitkanliGenetic Counseling (Geneva, Switzerland)|January 24, 2004
Moderate hearing loss and pseudodominant inheritance due to L90P/35delG mutations in the GJB2 (connexin 26) geneM Tekin, T Duman, G Boğoçlu, et al.Genetic Counseling (Geneva, Switzerland)|November 3, 2004
Balanced de novo translocation t(6;7)(p25;q31) and cleft palate as an isolated findingS Balci, E Aypar, Y Aydin Son, et al.Pageof 116