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K Keymolen

Showing results (1-10 of 25) with videos related to

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Journal of the European Academy of Dermatology and Venereology : JEADV|December 6, 2019
ERCC2 mutations in two siblings with a severe trichothiodystrophy phenotypeG Leemans, L De Raeve, K Keymolen
B-ENT|May 27, 2008
Pediatric tracheotomy: the Universitair Ziekenhuis Brussels' experienceL Gheyle, K Keymolen, S Halewijck, et al.
Genetic Counseling (Geneva, Switzerland)|January 13, 2000
Unilateral longitudinal radial ray deficiency of the hand and metacarpal 4-5 synostosisL De Smet, K Keymolen, J P Fryns
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|October 22, 2005
Intervention during pregnancy and allergic disease in the offspringS Salvatore, K Keymolen, B Hauser, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
How to counsel in osteopathia striata with cranial sclerosisK Keymolen, M Bonduelle, M De Maeseneer, et al.
Genetic Counseling (Geneva, Switzerland)|January 13, 2000
Segmentary fibrous dysplasia manifesting as macrodactylyK Keymolen, L De Smet, H Kenis, et al.
Genetic Counseling (Geneva, Switzerland)|November 5, 1999
The concurrence of ring constrictions in Adams-Oliver syndrome: additional evidence for vascular disruption as common pathogenetic mechanismK Keymolen, L De Smet, P Bracke, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 1, 1996
Symptomatology of Helicobacter pylori infection in childrenU Blecker, B Hauser, S Lanciers, et al.
Tijdschrift Voor Psychiatrie|July 6, 2007
[Mild mental retardation and complex psychiatric symptoms are accompanied by submicroscopic sub-telomeric deletion of a long arm of chromosome 3. A case study]H Kajosch, N Vanderbruggen, K Keymolen, et al.
American Journal of Medical Genetics|June 22, 2000
Distal limb deficiencies, oral involvement, and renal defect: report of a third patient and confirmation of a distinct entityK Keymolen, R Van Damme-Lombaerts, A Verloes, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Journal of the European Academy of Dermatology and Venereology : JEADV|December 6, 2019
ERCC2 mutations in two siblings with a severe trichothiodystrophy phenotypeG Leemans, L De Raeve, K Keymolen
B-ENT|May 27, 2008
Pediatric tracheotomy: the Universitair Ziekenhuis Brussels' experienceL Gheyle, K Keymolen, S Halewijck, et al.
Genetic Counseling (Geneva, Switzerland)|January 13, 2000
Unilateral longitudinal radial ray deficiency of the hand and metacarpal 4-5 synostosisL De Smet, K Keymolen, J P Fryns
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|October 22, 2005
Intervention during pregnancy and allergic disease in the offspringS Salvatore, K Keymolen, B Hauser, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
How to counsel in osteopathia striata with cranial sclerosisK Keymolen, M Bonduelle, M De Maeseneer, et al.
Genetic Counseling (Geneva, Switzerland)|January 13, 2000
Segmentary fibrous dysplasia manifesting as macrodactylyK Keymolen, L De Smet, H Kenis, et al.
Genetic Counseling (Geneva, Switzerland)|November 5, 1999
The concurrence of ring constrictions in Adams-Oliver syndrome: additional evidence for vascular disruption as common pathogenetic mechanismK Keymolen, L De Smet, P Bracke, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 1, 1996
Symptomatology of Helicobacter pylori infection in childrenU Blecker, B Hauser, S Lanciers, et al.
Tijdschrift Voor Psychiatrie|July 6, 2007
[Mild mental retardation and complex psychiatric symptoms are accompanied by submicroscopic sub-telomeric deletion of a long arm of chromosome 3. A case study]H Kajosch, N Vanderbruggen, K Keymolen, et al.
American Journal of Medical Genetics|June 22, 2000
Distal limb deficiencies, oral involvement, and renal defect: report of a third patient and confirmation of a distinct entityK Keymolen, R Van Damme-Lombaerts, A Verloes, et al.
Pageof 3