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J M Cobben

Showing results (1-10 of 63) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|July 26, 2005
[Lithium, a potentially dangerous drug]J M Cobben, D Lindhout
Clinical Dysmorphology|April 1, 1996
The EEC syndrome: a literature studyN M Roelfsema, J M Cobben
American Journal of Medical Genetics|April 27, 2002
SMN2 deletion in childhood-onset spinal muscular atrophyJ M Cobben, M de Visser
American Journal of Medical Genetics. Part A|April 25, 2013
Array CGH on unstimulated blood does not detect all cases of Pallister-Killian syndrome: buccal smear analysis should remain the diagnostic procedure of first choiceJ M Cobben, M Engelen, A Polstra
Nederlands Tijdschrift Voor Geneeskunde|January 17, 2002
[From gene to disease; 'survival' motor neuron protein and hereditary proximal spinal muscle atrophy]J M Cobben, M de Visser, H Scheffer
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Genetic counseling in limb reduction defectsJ M Cobben, S Hiemstra, P H Robinson
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|October 1, 1994
The popliteal pterygium syndrome: an analysis of two familiesP H Spauwen, J M Cobben, J W Gardeniers
European Journal of Human Genetics : EJHG|July 21, 2001
Best practice guidelines for molecular analysis in spinal muscular atrophyH Scheffer, J M Cobben, G Matthijs, et al.
Nederlands Tijdschrift Voor Geneeskunde|July 27, 1991
[DNA studies in proximal spinal muscular atrophy]J M Cobben, M de Visser, C H Buys
Fetal Diagnosis and Therapy|April 24, 2001
First trimester diagnosis of split hand/foot by transvaginal ultrasoundM C Haak, J M Cobben, J M van Vugt
Pageof 7

Showing results (1-10 of 63) with videos related to

Sort By:
Pageof 7
Nederlands Tijdschrift Voor Geneeskunde|July 26, 2005
[Lithium, a potentially dangerous drug]J M Cobben, D Lindhout
Clinical Dysmorphology|April 1, 1996
The EEC syndrome: a literature studyN M Roelfsema, J M Cobben
American Journal of Medical Genetics|April 27, 2002
SMN2 deletion in childhood-onset spinal muscular atrophyJ M Cobben, M de Visser
American Journal of Medical Genetics. Part A|April 25, 2013
Array CGH on unstimulated blood does not detect all cases of Pallister-Killian syndrome: buccal smear analysis should remain the diagnostic procedure of first choiceJ M Cobben, M Engelen, A Polstra
Nederlands Tijdschrift Voor Geneeskunde|January 17, 2002
[From gene to disease; 'survival' motor neuron protein and hereditary proximal spinal muscle atrophy]J M Cobben, M de Visser, H Scheffer
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Genetic counseling in limb reduction defectsJ M Cobben, S Hiemstra, P H Robinson
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|October 1, 1994
The popliteal pterygium syndrome: an analysis of two familiesP H Spauwen, J M Cobben, J W Gardeniers
European Journal of Human Genetics : EJHG|July 21, 2001
Best practice guidelines for molecular analysis in spinal muscular atrophyH Scheffer, J M Cobben, G Matthijs, et al.
Nederlands Tijdschrift Voor Geneeskunde|July 27, 1991
[DNA studies in proximal spinal muscular atrophy]J M Cobben, M de Visser, C H Buys
Fetal Diagnosis and Therapy|April 24, 2001
First trimester diagnosis of split hand/foot by transvaginal ultrasoundM C Haak, J M Cobben, J M van Vugt
Pageof 7