P Moerman|J P Fryns - JoVE Visualize

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Human Genetics|January 1, 1984

Cytogenetic survey in couples with recurrent fetal wastageJ P Fryns, A Kleczkowska, E Kubień, et al.

Genetic Counseling (Geneva, Switzerland)|October 20, 1998

Spasticity, mental retardation, macrocephaly and distinct craniofacial appearance: confirmation of a new subtype of complicated spastic paraplegia?U Moog, A M Schoonbrood-Lenssen, C T Schrander-Stumpel, et al.

American Journal of Human Genetics|November 9, 2000

Primary autosomal recessive microcephaly: MCPH5 maps to 1q25-q32C R Jamieson, J P Fryns, J Jacobs, et al.

Journal of Mental Deficiency Research|June 1, 1990

The 49,XXXXY syndrome: clinical and psychological findings in five patientsL M Curfs, G Schreppers-Tijdink, A Wiegers, et al.

Clinical Genetics|March 1, 1987

Tetraploidy with hydrops fetalis, cystic nuchal hygroma and 90, XX karyotypeJ P Fryns, K Vandenberghe, F Moerman, et al.

Acta Paediatrica Scandinavica|January 1, 1984

Complex chromosomal rearrangement in a mentally retarded boy without gross dysmorphic stigmataJ P Fryns, A Kleczkowska, E Lebas, et al.

Clinical Genetics|April 1, 1995

Variable expression of the popliteal pterygium syndrome in two 3-generation familiesD Soekarman, J M Cobben, A Vogels, et al.

Genetic Counseling (Geneva, Switzerland)|January 1, 1990

Cytogenetic findings in a consecutive series of 478 patients with Turner syndrome. The Leuven experience 1965-1989A Kleczkowska, E Dmoch, E Kubien, et al.

Human Genetics|October 31, 1978

Partial monosomy of the short arm of chromosome 9: a distinct clinical entityJ Deroover, J P Fryns, C Parloir, et al.

Humangenetik|May 26, 1975

Sex chromatin and cytogenetic survey of 10417 adult males and 357 children institutionalized in Belgian institutions for mentally retarded patientsJ J Cassiman, J P Fryns, J De Roover, et al.

Pageof 89

Showing results (491-500 of 883) with videos related to

Sort By:

Pageof 89

Human Genetics|January 1, 1984

Cytogenetic survey in couples with recurrent fetal wastageJ P Fryns, A Kleczkowska, E Kubień, et al.

Genetic Counseling (Geneva, Switzerland)|October 20, 1998

Spasticity, mental retardation, macrocephaly and distinct craniofacial appearance: confirmation of a new subtype of complicated spastic paraplegia?U Moog, A M Schoonbrood-Lenssen, C T Schrander-Stumpel, et al.

American Journal of Human Genetics|November 9, 2000

Primary autosomal recessive microcephaly: MCPH5 maps to 1q25-q32C R Jamieson, J P Fryns, J Jacobs, et al.

Journal of Mental Deficiency Research|June 1, 1990

The 49,XXXXY syndrome: clinical and psychological findings in five patientsL M Curfs, G Schreppers-Tijdink, A Wiegers, et al.

Clinical Genetics|March 1, 1987

Tetraploidy with hydrops fetalis, cystic nuchal hygroma and 90, XX karyotypeJ P Fryns, K Vandenberghe, F Moerman, et al.

Acta Paediatrica Scandinavica|January 1, 1984

Complex chromosomal rearrangement in a mentally retarded boy without gross dysmorphic stigmataJ P Fryns, A Kleczkowska, E Lebas, et al.

Clinical Genetics|April 1, 1995

Variable expression of the popliteal pterygium syndrome in two 3-generation familiesD Soekarman, J M Cobben, A Vogels, et al.

Genetic Counseling (Geneva, Switzerland)|January 1, 1990

Cytogenetic findings in a consecutive series of 478 patients with Turner syndrome. The Leuven experience 1965-1989A Kleczkowska, E Dmoch, E Kubien, et al.

Human Genetics|October 31, 1978

Partial monosomy of the short arm of chromosome 9: a distinct clinical entityJ Deroover, J P Fryns, C Parloir, et al.

Humangenetik|May 26, 1975

Sex chromatin and cytogenetic survey of 10417 adult males and 357 children institutionalized in Belgian institutions for mentally retarded patientsJ J Cassiman, J P Fryns, J De Roover, et al.

Pageof 89