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E Legius

Showing results (41-50 of 120) with videos related to

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Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Neurofibromatosis type 1E Legius, M J Descheemaeker, J P Fryns, et al.
European Journal of Pediatrics|August 1, 1989
Rickets due to dietary calcium deficiencyE Legius, W Proesmans, E Eggermont, et al.
European Journal of Pediatrics|June 1, 1990
Muscular hypertrophy of the oesophagus and "Alport-like" glomerular lesions in a boyE Legius, W Proesmans, B Van Damme, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|December 1, 1990
Alpha-1-proteinase inhibitor gene frequencies in BelgiumJ Kimpen, E Legius, E Bosmans, et al.
Genetic Counseling (Geneva, Switzerland)|January 23, 1999
Syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex)E Legius, W Daenen, V Vandenbergh, et al.
American Journal of Medical Genetics|August 28, 1995
Apparently new "anophthalmia-plus" syndrome in sibsJ P Fryns, E Legius, P Moerman, et al.
Human Molecular Genetics|April 18, 2000
Genetic and cellular defects contributing to benign tumor formation in neurofibromatosis type 1J L Rutkowski, K Wu, D H Gutmann, et al.
Gene|June 23, 2000
Characterization of the Fugu rubripes NLK and FN5 genes flanking the NF1 (Neurofibromatosis type 1) gene in the 5' direction and mapping of the human counterpartsH Kehrer-Sawatzki, E Moschgath, C Maier, et al.
Molecular Syndromology|August 3, 2012
NRAS Mutations in Noonan SyndromeE Denayer, H Peeters, L Sevenants, et al.
Human Mutation|January 1, 1996
Neurofibromatosis type I gene mutation in a patient with features of LEOPARD syndromeR Wu, E Legius, W Robberecht, et al.
Pageof 12

Showing results (41-50 of 120) with videos related to

Sort By:
Pageof 12
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Neurofibromatosis type 1E Legius, M J Descheemaeker, J P Fryns, et al.
European Journal of Pediatrics|August 1, 1989
Rickets due to dietary calcium deficiencyE Legius, W Proesmans, E Eggermont, et al.
European Journal of Pediatrics|June 1, 1990
Muscular hypertrophy of the oesophagus and "Alport-like" glomerular lesions in a boyE Legius, W Proesmans, B Van Damme, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|December 1, 1990
Alpha-1-proteinase inhibitor gene frequencies in BelgiumJ Kimpen, E Legius, E Bosmans, et al.
Genetic Counseling (Geneva, Switzerland)|January 23, 1999
Syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex)E Legius, W Daenen, V Vandenbergh, et al.
American Journal of Medical Genetics|August 28, 1995
Apparently new "anophthalmia-plus" syndrome in sibsJ P Fryns, E Legius, P Moerman, et al.
Human Molecular Genetics|April 18, 2000
Genetic and cellular defects contributing to benign tumor formation in neurofibromatosis type 1J L Rutkowski, K Wu, D H Gutmann, et al.
Gene|June 23, 2000
Characterization of the Fugu rubripes NLK and FN5 genes flanking the NF1 (Neurofibromatosis type 1) gene in the 5' direction and mapping of the human counterpartsH Kehrer-Sawatzki, E Moschgath, C Maier, et al.
Molecular Syndromology|August 3, 2012
NRAS Mutations in Noonan SyndromeE Denayer, H Peeters, L Sevenants, et al.
Human Mutation|January 1, 1996
Neurofibromatosis type I gene mutation in a patient with features of LEOPARD syndromeR Wu, E Legius, W Robberecht, et al.
Pageof 12