P Moerman|J P Fryns - JoVE Visualize

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

Neurofibromatosis type 1 in childhood: a study of the neuropsychological profile in 45 childrenE Legius, M J Descheemaeker, A Spaepen, et al.

Helvetica Paediatrica Acta|August 1, 1988

Mental retardation and Y/8 translocation [karyotype: 46,XY, t(Y;8)(q12;q24)] in father and sonJ P Fryns, A Kleczkowska, A M Dereymaeker, et al.

Clinical Genetics|July 1, 1987

Proximal duplication of the long arm of chromosome 10 (10q11.2----10q22): a distinct clinical entityJ P Fryns, A Kleczkowska, L Igodt-Ameye, et al.

Genetic Counseling (Geneva, Switzerland)|July 23, 2003

Partial monosomy 11q and trisomy 12q: variable expression in two siblingsT Lukusa, M Holvoet, J R Vermeesch, et al.

Genetic Counseling (Geneva, Switzerland)|May 3, 2001

Cystic hygroma colli as the first echographic sign of the fetal akinesia sequenceI Witters, P H Moerman, F A Van Assche, et al.

American Journal of Medical Genetics|August 10, 2001

PTEN mutation in a family with Cowden syndrome and autismA Goffin, L H Hoefsloot, E Bosgoed, et al.

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

Anterior basal encephalocele in the median cleft face syndrome. Comments on nosology and treatmentC Grubben, J P Fryns, F De Zegher, et al.

British Heart Journal|May 1, 1978

Cardiovascular malformations in Turner's and Noonan's syndromeL G Van der Hauwaert, J P Fryns, M Dumoulin, et al.

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

Neurofibromatosis type 1E Legius, M J Descheemaeker, J P Fryns, et al.

American Journal of Medical Genetics|July 1, 1992

Variability versus heterogeneity in syndromal hypothalamic hamartoblastoma and related disorders: review and delineation of the cerebro-acro-visceral early lethality (CAVE) multiplex syndromeA Verloes, Y Gillerot, J P Langhendries, et al.

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Showing results (421-430 of 883) with videos related to

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Pageof 89

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

Neurofibromatosis type 1 in childhood: a study of the neuropsychological profile in 45 childrenE Legius, M J Descheemaeker, A Spaepen, et al.

Helvetica Paediatrica Acta|August 1, 1988

Mental retardation and Y/8 translocation [karyotype: 46,XY, t(Y;8)(q12;q24)] in father and sonJ P Fryns, A Kleczkowska, A M Dereymaeker, et al.

Clinical Genetics|July 1, 1987

Proximal duplication of the long arm of chromosome 10 (10q11.2----10q22): a distinct clinical entityJ P Fryns, A Kleczkowska, L Igodt-Ameye, et al.

Genetic Counseling (Geneva, Switzerland)|July 23, 2003

Partial monosomy 11q and trisomy 12q: variable expression in two siblingsT Lukusa, M Holvoet, J R Vermeesch, et al.

Genetic Counseling (Geneva, Switzerland)|May 3, 2001

Cystic hygroma colli as the first echographic sign of the fetal akinesia sequenceI Witters, P H Moerman, F A Van Assche, et al.

American Journal of Medical Genetics|August 10, 2001

PTEN mutation in a family with Cowden syndrome and autismA Goffin, L H Hoefsloot, E Bosgoed, et al.

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

Anterior basal encephalocele in the median cleft face syndrome. Comments on nosology and treatmentC Grubben, J P Fryns, F De Zegher, et al.

British Heart Journal|May 1, 1978

Cardiovascular malformations in Turner's and Noonan's syndromeL G Van der Hauwaert, J P Fryns, M Dumoulin, et al.

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

Neurofibromatosis type 1E Legius, M J Descheemaeker, J P Fryns, et al.

American Journal of Medical Genetics|July 1, 1992

Variability versus heterogeneity in syndromal hypothalamic hamartoblastoma and related disorders: review and delineation of the cerebro-acro-visceral early lethality (CAVE) multiplex syndromeA Verloes, Y Gillerot, J P Langhendries, et al.

Pageof 89