P Moerman|J P Fryns - JoVE Visualize

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

Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p)P Petit, K Devriendt, J R Vermeesch, et al.

Journal of Medical Genetics|March 1, 1990

EEC syndrome without ectrodactyly: report of two new familiesJ P Fryns, E Legius, A M Dereymaeker, et al.

Prenatal Diagnosis|June 1, 1997

Diagnostic echographic findings in cryptophthalmos syndrome (Fraser syndrome)J P Fryns, D van Schoubroeck, K Vandenberghe, et al.

American Journal of Medical Genetics|July 15, 1994

Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream regionY Trottier, G Imbert, A Poustka, et al.

Genetic Counseling (Geneva, Switzerland)|January 1, 1994

Thrombocytopenia and cleft hand in monosomy 21A Vogels, L de Smet, H van den Berghe, et al.

Prenatal Diagnosis|February 17, 2001

Prenatal diagnosis of facial clefting as part of the oculo-auriculo-vertebral spectrumI Witters, J Schreurs, J Van Wing, et al.

Human Genetics|August 31, 1978

Malformative syndrome associated with a ring 10 chromosome and a translocated 10q/19 chromosomeJ P Fryns, K De Boeck, J Jaeken, et al.

Journal of Medical Genetics|February 25, 1998

Proteinuria in a patient with the diaphragmatic hernia-hypertelorism-myopia-deafness syndrome: further evidence that the facio-oculo-acoustico-renal syndrome represents the same entityK Devriendt, L Standaert, C Van Hole, et al.

Genetic Counseling (Geneva, Switzerland)|January 1, 1994

Personal independence of adult mentally retarded men with fragile-X syndromeB Maes, J P Fryns, M Van Walleghem, et al.

Human Genetics|November 10, 1977

Interstitial deletion of the long arm of chromosome 2 in a polymalformed newborn--karyotype: 46,XX,del(2)(q21;q24)J P Fryns, B Van Bosstraeten, H Malbrain, et al.

Pageof 89

Showing results (451-460 of 883) with videos related to

Sort By:

Pageof 89

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

Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p)P Petit, K Devriendt, J R Vermeesch, et al.

Journal of Medical Genetics|March 1, 1990

EEC syndrome without ectrodactyly: report of two new familiesJ P Fryns, E Legius, A M Dereymaeker, et al.

Prenatal Diagnosis|June 1, 1997

Diagnostic echographic findings in cryptophthalmos syndrome (Fraser syndrome)J P Fryns, D van Schoubroeck, K Vandenberghe, et al.

American Journal of Medical Genetics|July 15, 1994

Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream regionY Trottier, G Imbert, A Poustka, et al.

Genetic Counseling (Geneva, Switzerland)|January 1, 1994

Thrombocytopenia and cleft hand in monosomy 21A Vogels, L de Smet, H van den Berghe, et al.

Prenatal Diagnosis|February 17, 2001

Prenatal diagnosis of facial clefting as part of the oculo-auriculo-vertebral spectrumI Witters, J Schreurs, J Van Wing, et al.

Human Genetics|August 31, 1978

Malformative syndrome associated with a ring 10 chromosome and a translocated 10q/19 chromosomeJ P Fryns, K De Boeck, J Jaeken, et al.

Journal of Medical Genetics|February 25, 1998

Proteinuria in a patient with the diaphragmatic hernia-hypertelorism-myopia-deafness syndrome: further evidence that the facio-oculo-acoustico-renal syndrome represents the same entityK Devriendt, L Standaert, C Van Hole, et al.

Genetic Counseling (Geneva, Switzerland)|January 1, 1994

Personal independence of adult mentally retarded men with fragile-X syndromeB Maes, J P Fryns, M Van Walleghem, et al.

Human Genetics|November 10, 1977

Interstitial deletion of the long arm of chromosome 2 in a polymalformed newborn--karyotype: 46,XX,del(2)(q21;q24)J P Fryns, B Van Bosstraeten, H Malbrain, et al.

Pageof 89