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Genetic Counseling (Geneva, Switzerland)|April 29, 1998
Symbrachydactyly involving hands and feetL De Smet, G Fabry, J P FrynsGenetic Counseling (Geneva, Switzerland)|April 29, 1998
Oral-facial-digital syndrome type IV (Mohr-Majewski syndrome): a fetopathological studyP Moerman, J P FrynsGenetic Counseling (Geneva, Switzerland)|April 29, 1998
Diaphragmatic hernia in the Coffin-Siris syndromeV Delvaux, P Moerman, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1992
Which brain defects accompany cyclopia?I W Lurie, I A Kirillova, M K Nedzved, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1992
MCA/MR syndrome in two female siblings: new entity or variant examples of Coffin-Lowry versus Atkin-Flaitz syndromes?A Jans, E F Ippel, P F Dijkstra, et al.Genetic Counseling (Geneva, Switzerland)|May 3, 2001
Phenotypic variability of Cat-Eye syndromeM J Berends, G Tan-Sindhunata, B Leegte, et al.Genetic Counseling (Geneva, Switzerland)|May 3, 2001
De novo unbalanced t(11q;21q) leading to a partial monosomy 21pter-q22.2 and 11q24-qter in a patient initially diagnosed as monosomy 21M Riegel, A Baumer, A Piram, et al.Genetic Counseling (Geneva, Switzerland)|May 3, 2001
A maternal inherited translocation t(1;22)(q11;p11) in two infertile brothersI Lorda-Sanchez, C Tejedor, R Sanz, et al.Genetic Counseling (Geneva, Switzerland)|February 1, 2003
Dysmorphic face in two siblings with infantile neuroaxonal dystrophyM Seven, A Ozkiliç, A YükselGenetic Counseling (Geneva, Switzerland)|February 1, 2003
Small terminal 10q26 deletion in a male patient with Noonan-like stigmata: diagnosis by cytogenetic and FISH analysisT Lukusa, E Smeets, J R Vermeesch, et al.Pageof 116