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L C Wilson

Showing results (11-20 of 36) with videos related to

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American Journal of Medical Genetics|February 5, 1998
Choanal atresia and hypothelia following methimazole exposure in utero: a second reportL C Wilson, B A Kerr, R Wilkinson, et al.
Genomics|May 15, 1994
Characterization of a de novo 43-bp deletion of the Gs alpha gene (GNAS1) in Albright hereditary osteodystrophyM E Luttikhuis, L C Wilson, J V Leonard, et al.
Clinical Genetics|August 16, 2003
ROR2 is mutated in hereditary brachydactyly with nail dysplasia, but not in Sorsby syndromeC Bacchelli, L C Wilson, J A Cook, et al.
Archives of Biochemistry and Biophysics|May 1, 1990
Ascorbate protects against tert-butyl hydroperoxide inhibition of erythrocyte membrane Ca2+ + Mg2(+)-ATPaseR B Moore, A D Bamberg, L C Wilson, et al.
Clinical Genetics|November 4, 2004
Autosomal dominant B-cell immunodeficiency, distal limb anomalies and urogenital malformations (BILU syndrome) - report of a second familyM Tischkowitz, F Goodman, M Koliou, et al.
Journal of Medical Genetics|February 1, 1997
Normal erythrocyte membrane Gs alpha bioactivity in two unrelated patients with acrodysostosisL C Wilson, M E Oude Luttikhuis, M Baraitser, et al.
Molecular Pharmacology|March 22, 2001
Cyclooxygenase inhibitors regulate the expression of a TGF-beta superfamily member that has proapoptotic and antitumorigenic activitiesS J Baek, K S Kim, J B Nixon, et al.
Oncology|January 1, 1978
Californium Cf-252 for pelvic radiotherapyY Maruyama, J M Feola, D Tai, et al.
Journal of Medical Genetics|November 1, 1994
Parental origin of Gs alpha gene mutations in Albright's hereditary osteodystrophyL C Wilson, M E Oude Luttikhuis, P T Clayton, et al.
Clinical Dysmorphology|June 20, 2002
Hemifacial microsomia, external auditory canal atresia, deafness and Mullerian anomalies associated with acro-osteolysis: a new autosomal recessive syndrome?A F Brady, R M Winter, L C Wilson, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics|February 5, 1998
Choanal atresia and hypothelia following methimazole exposure in utero: a second reportL C Wilson, B A Kerr, R Wilkinson, et al.
Genomics|May 15, 1994
Characterization of a de novo 43-bp deletion of the Gs alpha gene (GNAS1) in Albright hereditary osteodystrophyM E Luttikhuis, L C Wilson, J V Leonard, et al.
Clinical Genetics|August 16, 2003
ROR2 is mutated in hereditary brachydactyly with nail dysplasia, but not in Sorsby syndromeC Bacchelli, L C Wilson, J A Cook, et al.
Archives of Biochemistry and Biophysics|May 1, 1990
Ascorbate protects against tert-butyl hydroperoxide inhibition of erythrocyte membrane Ca2+ + Mg2(+)-ATPaseR B Moore, A D Bamberg, L C Wilson, et al.
Clinical Genetics|November 4, 2004
Autosomal dominant B-cell immunodeficiency, distal limb anomalies and urogenital malformations (BILU syndrome) - report of a second familyM Tischkowitz, F Goodman, M Koliou, et al.
Journal of Medical Genetics|February 1, 1997
Normal erythrocyte membrane Gs alpha bioactivity in two unrelated patients with acrodysostosisL C Wilson, M E Oude Luttikhuis, M Baraitser, et al.
Molecular Pharmacology|March 22, 2001
Cyclooxygenase inhibitors regulate the expression of a TGF-beta superfamily member that has proapoptotic and antitumorigenic activitiesS J Baek, K S Kim, J B Nixon, et al.
Oncology|January 1, 1978
Californium Cf-252 for pelvic radiotherapyY Maruyama, J M Feola, D Tai, et al.
Journal of Medical Genetics|November 1, 1994
Parental origin of Gs alpha gene mutations in Albright's hereditary osteodystrophyL C Wilson, M E Oude Luttikhuis, P T Clayton, et al.
Clinical Dysmorphology|June 20, 2002
Hemifacial microsomia, external auditory canal atresia, deafness and Mullerian anomalies associated with acro-osteolysis: a new autosomal recessive syndrome?A F Brady, R M Winter, L C Wilson, et al.
Pageof 4