J J P Gille - JoVE Visualize

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Nederlands Tijdschrift Voor Geneeskunde|May 12, 2005

[From gene to disease; EVC, EVC2, and Ellis-van Creveld syndrome]J M van Hagen, J A Baart, J J P Gille

Breast Cancer Research and Treatment|June 29, 2010

PALB2 analysis in BRCA2-like familiesM A Adank, S E van Mil, J J P Gille, et al.

Prenatal Diagnosis|November 27, 2004

Improved prenatal detection of a fetal point mutation for achondroplasia by the use of size-fractionated circulatory DNA in maternal plasma--case reportY Li, W Holzgreve, G C M L Page-Christiaens, et al.

Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|October 25, 2011

Genetic counselling for pulmonary arterial hypertension: a matter of variable variabilityE M Leter, A B Boonstra, F B Postma, et al.

Journal of Clinical Pathology|October 2, 2002

Multiple fibroadenomas harbouring carcinoma in situ in a woman with a family history of breast/ovarian cancerA Kuijper, S S Preisler-Adams, F D Rahusen, 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.

Nederlands Tijdschrift Voor Geneeskunde|February 4, 2005

[From gene to disease: basal cell naevus syndrome]T G J de Meij, M J H Baars, J J P Gille, et al.

American Journal of Medical Genetics. Part A|July 15, 2005

Interstitial deletion in 3q in a patient with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) and microcephaly, mild mental retardation and growth delay: clinical report and review of the literatureM H de Ru, J J P Gille, A W M Nieuwint, et al.

Journal of Intellectual Disability Research : JIDR|January 5, 2008

Feasibility and outcomes of multiplex ligation-dependent probe amplification on buccal smears as a screening method for microdeletions and duplications among 300 adults with an intellectual disability of unknown aetiologyD Peppink, D D Douma-Kloppenburg, E S P de Rooij-Askes, et al.

Histopathology|June 26, 2003

Expression of differentiation and proliferation related proteins in epithelium of prophylactically removed ovaries from women with a hereditary female adnexal cancer predispositionJ M J Piek, R H M Verheijen, F H Menko, et al.

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Showing results (1-10 of 28) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|May 12, 2005

[From gene to disease; EVC, EVC2, and Ellis-van Creveld syndrome]J M van Hagen, J A Baart, J J P Gille

Breast Cancer Research and Treatment|June 29, 2010

PALB2 analysis in BRCA2-like familiesM A Adank, S E van Mil, J J P Gille, et al.

Prenatal Diagnosis|November 27, 2004

Improved prenatal detection of a fetal point mutation for achondroplasia by the use of size-fractionated circulatory DNA in maternal plasma--case reportY Li, W Holzgreve, G C M L Page-Christiaens, et al.

Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|October 25, 2011

Genetic counselling for pulmonary arterial hypertension: a matter of variable variabilityE M Leter, A B Boonstra, F B Postma, et al.

Journal of Clinical Pathology|October 2, 2002

Multiple fibroadenomas harbouring carcinoma in situ in a woman with a family history of breast/ovarian cancerA Kuijper, S S Preisler-Adams, F D Rahusen, 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.

Nederlands Tijdschrift Voor Geneeskunde|February 4, 2005

[From gene to disease: basal cell naevus syndrome]T G J de Meij, M J H Baars, J J P Gille, et al.

American Journal of Medical Genetics. Part A|July 15, 2005

Interstitial deletion in 3q in a patient with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) and microcephaly, mild mental retardation and growth delay: clinical report and review of the literatureM H de Ru, J J P Gille, A W M Nieuwint, et al.

Journal of Intellectual Disability Research : JIDR|January 5, 2008

Feasibility and outcomes of multiplex ligation-dependent probe amplification on buccal smears as a screening method for microdeletions and duplications among 300 adults with an intellectual disability of unknown aetiologyD Peppink, D D Douma-Kloppenburg, E S P de Rooij-Askes, et al.

Histopathology|June 26, 2003

Expression of differentiation and proliferation related proteins in epithelium of prophylactically removed ovaries from women with a hereditary female adnexal cancer predispositionJ M J Piek, R H M Verheijen, F H Menko, et al.

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