P Moerman|J P Fryns - JoVE Visualize

Showing results (21-30 of 883) with videos related to

Pageof 89

Sort By:

The Journal of Pediatrics|August 1, 1983

Multiple ankyloses, facial anomalies, and pulmonary hypoplasia associated with severe antenatal spinal muscular atrophyP Moerman, J P Fryns, P Goddeeris, et al.

Pediatric Pathology|January 1, 1985

Primitive neuroectodermal tumor: a newly recognized cause of early fetal deathP Moerman, P Goddeeris, J P Fryns, et al.

Clinical Genetics|September 4, 1998

Marden-Walker syndrome versus isolated distal arthrogryposis: evidence that both conditions may be variable manifestations of the same mutated geneJ P Fryns, D Willekens, D Van Schoubroeck, et al.

American Journal of Medical Genetics|February 15, 1992

Constrictive amniotic bands, amniotic adhesions, and limb-body wall complex: discrete disruption sequences with pathogenetic overlapP Moerman, J P Fryns, K Vandenberghe, et al.

Prenatal Diagnosis|January 13, 1999

Prenatal diagnosis of de novo distal 5q duplication associated with hygroma colli, fetal oedema and complex cardiopathyI Witters, G Van Buggenhout, P Moerman, et al.

Journal De Genetique Humaine|March 1, 1982

Spectrum of clinical and autopsy findings in trisomy 18 syndromeP Moerman, J P Fryns, P Goddeeris, et al.

Pediatrics|April 1, 1984

Pathogenesis of the prune-belly syndrome: a functional urethral obstruction caused by prostatic hypoplasiaP Moerman, J P Fryns, P Goddeeris, et al.

Archives of Pathology & Laboratory Medicine|November 1, 1982

Nonimmunologic hydrops fetalis. A study of ten casesP Moerman, J P Fryns, P Goddeeris, et al.

Journal De Genetique Humaine|September 1, 1989

[A new sublethal syndrome with multiple malformations associating diaphragmatic hernia, distal digital hypoplasia, and craniofacial anomalies. The "Fryns syndrome"]J P Fryns, P Moerman, H Van den Berghe, et al.

Genetic Counseling (Geneva, Switzerland)|January 1, 1992

Tetraphocomelia and bilateral femorotibial synostosis. A severe variant of the thrombocytopenia-absent radii (TAR) syndrome?J Delooz, P Moerman, K Van den Berghe, et al.

Pageof 89

Showing results (21-30 of 883) with videos related to

Sort By:

Pageof 89

The Journal of Pediatrics|August 1, 1983

Multiple ankyloses, facial anomalies, and pulmonary hypoplasia associated with severe antenatal spinal muscular atrophyP Moerman, J P Fryns, P Goddeeris, et al.

Pediatric Pathology|January 1, 1985

Primitive neuroectodermal tumor: a newly recognized cause of early fetal deathP Moerman, P Goddeeris, J P Fryns, et al.

Clinical Genetics|September 4, 1998

Marden-Walker syndrome versus isolated distal arthrogryposis: evidence that both conditions may be variable manifestations of the same mutated geneJ P Fryns, D Willekens, D Van Schoubroeck, et al.

American Journal of Medical Genetics|February 15, 1992

Constrictive amniotic bands, amniotic adhesions, and limb-body wall complex: discrete disruption sequences with pathogenetic overlapP Moerman, J P Fryns, K Vandenberghe, et al.

Prenatal Diagnosis|January 13, 1999

Prenatal diagnosis of de novo distal 5q duplication associated with hygroma colli, fetal oedema and complex cardiopathyI Witters, G Van Buggenhout, P Moerman, et al.

Journal De Genetique Humaine|March 1, 1982

Spectrum of clinical and autopsy findings in trisomy 18 syndromeP Moerman, J P Fryns, P Goddeeris, et al.

Pediatrics|April 1, 1984

Pathogenesis of the prune-belly syndrome: a functional urethral obstruction caused by prostatic hypoplasiaP Moerman, J P Fryns, P Goddeeris, et al.

Archives of Pathology & Laboratory Medicine|November 1, 1982

Nonimmunologic hydrops fetalis. A study of ten casesP Moerman, J P Fryns, P Goddeeris, et al.

Journal De Genetique Humaine|September 1, 1989

[A new sublethal syndrome with multiple malformations associating diaphragmatic hernia, distal digital hypoplasia, and craniofacial anomalies. The "Fryns syndrome"]J P Fryns, P Moerman, H Van den Berghe, et al.

Genetic Counseling (Geneva, Switzerland)|January 1, 1992

Tetraphocomelia and bilateral femorotibial synostosis. A severe variant of the thrombocytopenia-absent radii (TAR) syndrome?J Delooz, P Moerman, K Van den Berghe, et al.

Pageof 89