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Martinus F Niermeijer

Showing results (1-10 of 15) with videos related to

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The Lancet. Oncology|October 3, 2006
Preimplantation genetic diagnosis for cancerMartinus F Niermeijer, Guido de Wert, Wybo Dondorp
JAMA|May 24, 2012
Genomic sequencing in newborn screening programsWybo J Dondorp, Guido M W R de Wert, Martinus F Niermeijer
Clinical Dysmorphology|May 11, 2002
Kabuki syndrome: a review study of three hundred patientsMarja W Wessels, Alice S Brooks, Jeannette Hoogeboom, et al.
American Journal of Medical Genetics|September 5, 2002
Another family with nonspecific X-linked mental retardation (MRX78) maps to Xp11.4-p11.23Bert B A de Vries, Guido J Breedveld, Wouter H Deelen, et al.
Menopause (New York, N.Y.)|April 17, 2010
Similar phenotype characteristics comparing familial and sporadic premature ovarian failureFemi Janse, Erik A H Knauff, Martinus F Niermeijer, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|January 26, 2006
No evidence for large-scale germline genomic aberrations in hereditary bladder cancer patients with high-resolution array-based comparative genomic hybridizationLambertus A Kiemeney, Roland P Kuiper, Rolph Pfundt, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
Familial gigantism caused by an NSD1 mutationMieke M van Haelst, Jeannette J M Hoogeboom, Genevieve Baujat, et al.
Annals of Neurology|March 14, 2002
A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's diseaseSonia M Rosso, Esther van Herpen, Wout Deelen, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
Attitudes and distress levels in women at risk to carry a BRCA1/BRCA2 gene mutation who decline genetic testingLitanja Lodder, Petra G Frets, R Willem Trijsburg, et al.
American Journal of Medical Genetics. Part A|November 6, 2004
Three new families with arterial tortuosity syndromeMarja W Wessels, Coriene E Catsman-Berrevoets, Grazia M S Mancini, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
The Lancet. Oncology|October 3, 2006
Preimplantation genetic diagnosis for cancerMartinus F Niermeijer, Guido de Wert, Wybo Dondorp
JAMA|May 24, 2012
Genomic sequencing in newborn screening programsWybo J Dondorp, Guido M W R de Wert, Martinus F Niermeijer
Clinical Dysmorphology|May 11, 2002
Kabuki syndrome: a review study of three hundred patientsMarja W Wessels, Alice S Brooks, Jeannette Hoogeboom, et al.
American Journal of Medical Genetics|September 5, 2002
Another family with nonspecific X-linked mental retardation (MRX78) maps to Xp11.4-p11.23Bert B A de Vries, Guido J Breedveld, Wouter H Deelen, et al.
Menopause (New York, N.Y.)|April 17, 2010
Similar phenotype characteristics comparing familial and sporadic premature ovarian failureFemi Janse, Erik A H Knauff, Martinus F Niermeijer, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|January 26, 2006
No evidence for large-scale germline genomic aberrations in hereditary bladder cancer patients with high-resolution array-based comparative genomic hybridizationLambertus A Kiemeney, Roland P Kuiper, Rolph Pfundt, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
Familial gigantism caused by an NSD1 mutationMieke M van Haelst, Jeannette J M Hoogeboom, Genevieve Baujat, et al.
Annals of Neurology|March 14, 2002
A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's diseaseSonia M Rosso, Esther van Herpen, Wout Deelen, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
Attitudes and distress levels in women at risk to carry a BRCA1/BRCA2 gene mutation who decline genetic testingLitanja Lodder, Petra G Frets, R Willem Trijsburg, et al.
American Journal of Medical Genetics. Part A|November 6, 2004
Three new families with arterial tortuosity syndromeMarja W Wessels, Coriene E Catsman-Berrevoets, Grazia M S Mancini, et al.
Pageof 2