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Human Genetics|May 16, 1978
Familial occurrence of severe ulnar aplasia and lobster claw feet: a new syndromeH van den Berghe, J Dequeker, J P Fryns, et al.Clinical Genetics|August 1, 1982
Fertility in patients with X chromosome deletionsJ P Fryns, A Kleczkowska, P Petit, et al.Clinical Genetics|October 1, 1996
Distinct facial appearance with nasal hypoplasia, constipation, severe mental retardation and hypotonia in two unrelated young malesJ P Fryns, C De Troch, C Van Mol, et al.Annales De Genetique|January 1, 1992
Transmission of ring chromosome 18 46,XX/46,XX,r(18) mosaicism in a mother and ring chromosome 18 syndrome in her sonJ P Fryns, A Kleczkowska, E Smeets, et al.Acta Paediatrica Scandinavica. Supplement|January 1, 1984
Cytogenetic findings in moderate and severe mental retardation. A study of an institutionalized population of 1991 patientsJ P Fryns, A Kleczkowska, E Kubień, et al.Annales De Genetique|January 1, 1985
De novo partial 2q3 trisomy/distal 7p22 monosomy in a malformed newborn with 7p deletion phenotype and craniosynostosisJ P Fryns, M Haspeslagh, A Agneessens, et al.Annales De Genetique|January 1, 1985
Unusual chromosome 9 polymorphism and reproductive failureJ P Fryns, A Kleczkowska, L Londers, et al.Human Genetics|June 19, 1979
Paracentric inversion in the short arm of chromosome 1J Deroover, J P Fryns, J Haegeman, et al.Human Genetics|June 30, 1977
Full monosomy 21: a clinically recognizable syndrome?J P Fryns, F D'Hondt, P Goddeeris, et al.Genetic Counseling (Geneva, Switzerland)|January 31, 2006
Partial trisomy 9q syndrome with a de novo tandem duplication of 9q22.2-q31.1G E Utine, C Melotte, J R Vermeesch, et al.Pageof 89