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M L Kwee

Showing results (1-10 of 26) with videos related to

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American Journal of Medical Genetics|July 1, 1988
Inheritance of cranio-fronto-nasal syndromeM L Kwee, D Lindhout
Clinical Genetics|July 1, 1984
Craniofrontonasal dysplasia: genetic heterogeneity?M L Kwee, D Lindhout
Clinical Genetics|September 1, 1983
Frontonasal dysplasia, coronal craniosynostosis, pre- and postaxial polydactyly and split nails: a new autosomal dominant mutant with reduced penetrance and variable expression?M L Kwee, D Lindhout
Ophthalmic Paediatrics and Genetics|June 1, 1990
Tuberous sclerosis. Diagnostic problems in a familyD B van Dorp, M L Kwee
Nederlands Tijdschrift Voor Geneeskunde|October 20, 1979
[Listeria monocytogenes in newborn infants; an organism causing sepsis and meningitis]M L Kwee, S Soepatmi, J G Koppe
Clinical Genetics|August 1, 1984
Mosaic tetrasomy 21 in a male childM L Kwee, P G Barth, F Arwert, et al.
American Journal of Medical Genetics|October 21, 1998
Confounding factors in the diagnosis of Fanconi anaemiaH Joenje, F Arwert, M L Kwee, et al.
The Cleft Palate Journal|July 1, 1988
Van der Woude syndrome--recognition of lesser expressions: case reportF H Menko, P H Koedijk, J A Baart, et al.
Parkinsonism & Related Disorders|October 20, 2006
First case of ataxia with isolated vitamin E deficiency in the NetherlandsS C Ponten, M L Kwee, E Ch Wolters, et al.
Nederlands Tijdschrift Voor Geneeskunde|December 30, 2006
[A Dutch family with the hereditary periodic fever or tumour necrosis factor receptor-associated periodic syndrome (TRAPS)]N M N J Chang Pan Huo, J E Dankert-Roelse, M L Kwee
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|July 1, 1988
Inheritance of cranio-fronto-nasal syndromeM L Kwee, D Lindhout
Clinical Genetics|July 1, 1984
Craniofrontonasal dysplasia: genetic heterogeneity?M L Kwee, D Lindhout
Clinical Genetics|September 1, 1983
Frontonasal dysplasia, coronal craniosynostosis, pre- and postaxial polydactyly and split nails: a new autosomal dominant mutant with reduced penetrance and variable expression?M L Kwee, D Lindhout
Ophthalmic Paediatrics and Genetics|June 1, 1990
Tuberous sclerosis. Diagnostic problems in a familyD B van Dorp, M L Kwee
Nederlands Tijdschrift Voor Geneeskunde|October 20, 1979
[Listeria monocytogenes in newborn infants; an organism causing sepsis and meningitis]M L Kwee, S Soepatmi, J G Koppe
Clinical Genetics|August 1, 1984
Mosaic tetrasomy 21 in a male childM L Kwee, P G Barth, F Arwert, et al.
American Journal of Medical Genetics|October 21, 1998
Confounding factors in the diagnosis of Fanconi anaemiaH Joenje, F Arwert, M L Kwee, et al.
The Cleft Palate Journal|July 1, 1988
Van der Woude syndrome--recognition of lesser expressions: case reportF H Menko, P H Koedijk, J A Baart, et al.
Parkinsonism & Related Disorders|October 20, 2006
First case of ataxia with isolated vitamin E deficiency in the NetherlandsS C Ponten, M L Kwee, E Ch Wolters, et al.
Nederlands Tijdschrift Voor Geneeskunde|December 30, 2006
[A Dutch family with the hereditary periodic fever or tumour necrosis factor receptor-associated periodic syndrome (TRAPS)]N M N J Chang Pan Huo, J E Dankert-Roelse, M L Kwee
Pageof 3