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M L Kwee

Showing results (11-20 of 26) with videos related to

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Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|June 17, 2005
Camurati-Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan familyS Simsek, K Janssens, M L Kwee, et al.
American Journal of Medical Genetics|July 1, 1991
Joubert syndrome: a clinical and pathological description of an affected male and a female fetus from the same sibshipD B van Dorp, A Palan, M L Kwee, et al.
The British Journal of Dermatology|January 1, 1992
Clinical features of an affected father and daughter with Ehlers-Danlos syndrome type VIIBF M Pope, A C Nicholls, A Palan, et al.
Clinical Neurology and Neurosurgery|January 1, 1982
H-reflex studies in a family with possibly X-linked neuronal Charcot-Marie-Tooth diseaseJ J Heimans, D Lindhout, U W Huisman, et al.
Ophthalmic Genetics|April 26, 2000
Kabuki syndrome - report of six cases and review of the literature with emphasis on ocular featuresI Kluijt, D B van Dorp, M L Kwee, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Kabuki syndrome in son and low grade mosaic 45,X/46,XX in motherJ M Van Hagen, M L Kwee, K Madan, et al.
Teratology|April 1, 1993
Acardius acephalus after induced ovulation: a case reportD A Haring, M C Cornel, J C van der Linden, et al.
Human Genetics|January 1, 1983
Unusual response to bifunctional alkylating agents in a case of Fanconi anaemiaM L Kwee, E H Poll, J J van de Kamp, et al.
American Journal of Medical Genetics. Part A|July 21, 2004
Mesomelic dysplasia, Kantaputra type: clinical report, prenatal diagnosis, no evidence for SHOX deletion/mutationM L Kwee, J A van de Sluijs, J M G van Vugt, et al.
American Journal of Medical Genetics|January 31, 1997
An atypical case of Fanconi anemia in elderly sibsM L Kwee, J M van der Kleij, A J van Essen, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|June 17, 2005
Camurati-Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan familyS Simsek, K Janssens, M L Kwee, et al.
American Journal of Medical Genetics|July 1, 1991
Joubert syndrome: a clinical and pathological description of an affected male and a female fetus from the same sibshipD B van Dorp, A Palan, M L Kwee, et al.
The British Journal of Dermatology|January 1, 1992
Clinical features of an affected father and daughter with Ehlers-Danlos syndrome type VIIBF M Pope, A C Nicholls, A Palan, et al.
Clinical Neurology and Neurosurgery|January 1, 1982
H-reflex studies in a family with possibly X-linked neuronal Charcot-Marie-Tooth diseaseJ J Heimans, D Lindhout, U W Huisman, et al.
Ophthalmic Genetics|April 26, 2000
Kabuki syndrome - report of six cases and review of the literature with emphasis on ocular featuresI Kluijt, D B van Dorp, M L Kwee, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Kabuki syndrome in son and low grade mosaic 45,X/46,XX in motherJ M Van Hagen, M L Kwee, K Madan, et al.
Teratology|April 1, 1993
Acardius acephalus after induced ovulation: a case reportD A Haring, M C Cornel, J C van der Linden, et al.
Human Genetics|January 1, 1983
Unusual response to bifunctional alkylating agents in a case of Fanconi anaemiaM L Kwee, E H Poll, J J van de Kamp, et al.
American Journal of Medical Genetics. Part A|July 21, 2004
Mesomelic dysplasia, Kantaputra type: clinical report, prenatal diagnosis, no evidence for SHOX deletion/mutationM L Kwee, J A van de Sluijs, J M G van Vugt, et al.
American Journal of Medical Genetics|January 31, 1997
An atypical case of Fanconi anemia in elderly sibsM L Kwee, J M van der Kleij, A J van Essen, et al.
Pageof 3