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N Van Regemorter

Showing results (41-50 of 71) with videos related to

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Neuropediatrics|October 1, 1995
Mid-portion agenesis of corpus callosum in a presumed Baller-Gerold syndromeA Dunac, P Van Bogaert, P David, et al.
Fetal Diagnosis and Therapy|May 1, 1995
Cordocentesis for rapid karyotype: 421 consecutive casesC Donner, F Rypens, V Paquet, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
A D255H substitution in the arylsulphatase A gene of two unrelated Belgian patients with late-infantile metachromatic leukodystrophyW Lissens, R Vervoort, N Van Regemorter, et al.
The Journal of Pediatrics|March 1, 1984
Congenital malformations in 10,000 consecutive births in a university hospital: need for genetic counseling and prenatal diagnosisN Van Regemorter, J Dodion, C Druart, et al.
American Journal of Medical Genetics|April 10, 1995
Severe Smith-Lemli-Opitz syndrome with prolonged survival and lipid abnormalitiesG Pierquin, P Peeters, F Roels, et al.
European Journal of Pediatrics|February 1, 1982
Holt Oram syndrome mistaken for thalidomide embryopathy--embryological considerationsN Van Regemorter, D Haumont, C Kirkpatrick, et al.
Journal De Genetique Humaine|September 1, 1985
[S-100 protein in amniotic fluid of the ancencephalic fetus]M Freund, C J Sindic, N Van Regemorter, et al.
American Journal of Human Genetics|October 16, 1999
A new neurological syndrome with mental retardation, choreoathetosis, and abnormal behavior maps to chromosome Xp11E Reyniers, P Van Bogaert, N Peeters, et al.
Progress in Clinical and Biological Research|January 1, 1982
Spondyloepiphyseal dysplasia congenita: case reportN Van Regemorter, M Rooze, J Milaire, et al.
Acta Obstetricia Et Gynecologica Scandinavica|January 1, 1986
Pathological pregnancies. Results of amniotic fluid studies and fetal outcomeN Van Regemorter, E Vamos, V Defleur, et al.
Pageof 8

Showing results (41-50 of 71) with videos related to

Sort By:
Pageof 8
Neuropediatrics|October 1, 1995
Mid-portion agenesis of corpus callosum in a presumed Baller-Gerold syndromeA Dunac, P Van Bogaert, P David, et al.
Fetal Diagnosis and Therapy|May 1, 1995
Cordocentesis for rapid karyotype: 421 consecutive casesC Donner, F Rypens, V Paquet, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
A D255H substitution in the arylsulphatase A gene of two unrelated Belgian patients with late-infantile metachromatic leukodystrophyW Lissens, R Vervoort, N Van Regemorter, et al.
The Journal of Pediatrics|March 1, 1984
Congenital malformations in 10,000 consecutive births in a university hospital: need for genetic counseling and prenatal diagnosisN Van Regemorter, J Dodion, C Druart, et al.
American Journal of Medical Genetics|April 10, 1995
Severe Smith-Lemli-Opitz syndrome with prolonged survival and lipid abnormalitiesG Pierquin, P Peeters, F Roels, et al.
European Journal of Pediatrics|February 1, 1982
Holt Oram syndrome mistaken for thalidomide embryopathy--embryological considerationsN Van Regemorter, D Haumont, C Kirkpatrick, et al.
Journal De Genetique Humaine|September 1, 1985
[S-100 protein in amniotic fluid of the ancencephalic fetus]M Freund, C J Sindic, N Van Regemorter, et al.
American Journal of Human Genetics|October 16, 1999
A new neurological syndrome with mental retardation, choreoathetosis, and abnormal behavior maps to chromosome Xp11E Reyniers, P Van Bogaert, N Peeters, et al.
Progress in Clinical and Biological Research|January 1, 1982
Spondyloepiphyseal dysplasia congenita: case reportN Van Regemorter, M Rooze, J Milaire, et al.
Acta Obstetricia Et Gynecologica Scandinavica|January 1, 1986
Pathological pregnancies. Results of amniotic fluid studies and fetal outcomeN Van Regemorter, E Vamos, V Defleur, et al.
Pageof 8