P Moerman|J P Fryns - JoVE Visualize

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Journal of Medical Genetics|August 1, 1993

Origins of the fragile X syndrome mutationM C Hirst, S J Knight, Z Christodoulou, et al.

Genetic Counseling (Geneva, Switzerland)|April 16, 2004

Report of two Turkish infants with Norman-Roberts syndromeH Caksen, O Tuncer, E Kirimi, et al.

Genomics|December 1, 1996

Structure, sequence, and chromosome 19 localization of human USF2 and its rearrangement in a patient with multicystic renal dysplasiaP M Groenen, E Garcia, P Debeer, et al.

Annales De Genetique|January 9, 1999

Zygodactyly as the most striking physical anomaly in an adult male patient with pure partial trisomy 1qT Lukusa, G Van Buggenhout, K Devriendt, et al.

Experimental and Therapeutic Medicine|September 21, 2012

Curcumin for the prevention of progression in monoclonal gammopathy of undetermined significance: A word of cautionA J M Vermorken, J Zhu, W J M VAN DE Ven, et al.

Clinical Genetics|December 17, 2009

DISC1 duplication in two brothers with autism and mild mental retardationA Crepel, J Breckpot, J-P Fryns, et al.

Annales De Genetique|January 1, 1983

XY/XXY mosaicism and fragile X syndromeJ P Fryns, A Kleczkowska, E Kubień, et al.

Bulletin De La Societe Belge D'Ophtalmologie|February 5, 2003

Ophthalmological findings in a patient with mucolipidosis III (pseudo-hurler polydystrophy). A case reportS Pourjavan, J P Fryns, J L K Van Hove, et al.

Clinical Genetics|May 1, 1996

Cohen syndrome: the clinical symptoms and stigmata at a young ageJ P Fryns, E Legius, K Devriendt, et al.

Genetic Counseling (Geneva, Switzerland)|January 1, 1996

Partial trisomy and partial monosomy of the distal long arm of chromosome 4: patient report and literature reviewS G Frints, C T Schrander-Stumpel, J J Engelen, et al.

Pageof 89

Showing results (681-690 of 883) with videos related to

Sort By:

Pageof 89

Journal of Medical Genetics|August 1, 1993

Origins of the fragile X syndrome mutationM C Hirst, S J Knight, Z Christodoulou, et al.

Genetic Counseling (Geneva, Switzerland)|April 16, 2004

Report of two Turkish infants with Norman-Roberts syndromeH Caksen, O Tuncer, E Kirimi, et al.

Genomics|December 1, 1996

Structure, sequence, and chromosome 19 localization of human USF2 and its rearrangement in a patient with multicystic renal dysplasiaP M Groenen, E Garcia, P Debeer, et al.

Annales De Genetique|January 9, 1999

Zygodactyly as the most striking physical anomaly in an adult male patient with pure partial trisomy 1qT Lukusa, G Van Buggenhout, K Devriendt, et al.

Experimental and Therapeutic Medicine|September 21, 2012

Curcumin for the prevention of progression in monoclonal gammopathy of undetermined significance: A word of cautionA J M Vermorken, J Zhu, W J M VAN DE Ven, et al.

Clinical Genetics|December 17, 2009

DISC1 duplication in two brothers with autism and mild mental retardationA Crepel, J Breckpot, J-P Fryns, et al.

Annales De Genetique|January 1, 1983

XY/XXY mosaicism and fragile X syndromeJ P Fryns, A Kleczkowska, E Kubień, et al.

Bulletin De La Societe Belge D'Ophtalmologie|February 5, 2003

Ophthalmological findings in a patient with mucolipidosis III (pseudo-hurler polydystrophy). A case reportS Pourjavan, J P Fryns, J L K Van Hove, et al.

Clinical Genetics|May 1, 1996

Cohen syndrome: the clinical symptoms and stigmata at a young ageJ P Fryns, E Legius, K Devriendt, et al.

Genetic Counseling (Geneva, Switzerland)|January 1, 1996

Partial trisomy and partial monosomy of the distal long arm of chromosome 4: patient report and literature reviewS G Frints, C T Schrander-Stumpel, J J Engelen, et al.

Pageof 89