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Martijn H Breuning

Showing results (1-10 of 112) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|April 21, 2009
[Genetic associate studies in multifactorial genetic diseases]Martijn H Breuning
European Journal of Human Genetics : EJHG|February 24, 2005
Genetic Testing: from chromosomes to DNA, a revolution in prenatal diagnosisMartijn H Breuning
The New England Journal of Medicine|January 6, 2012
Case 26-2011: A boy with a complex kidney cystMartijn H Breuning
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2015
Response to Dalal et alKamlesh Madan, Martijn H Breuning
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 2, 2013
Impact of prenatal technologies on the sex ratio in India: an overviewKamlesh Madan, Martijn H Breuning
Methods in Cell Biology|December 18, 2004
Detecting copy number changes in genomic DNA: MAPH and MLPAStefan J White, Martijn H Breuning, Johan T den Dunnen
Pediatric Endocrinology Reviews : PER|April 28, 2009
Overgrowth syndromes:from classical to newRemco Visser, Sarina G Kant, Jan M Wit, et al.
European Journal of Human Genetics : EJHG|March 3, 2005
Unclassified variants in disease-causing genes: nonuniformity of genetic testing and counselling, a proposal for guidelinesGeraldine R Vink, Christi J van Asperen, Peter Devilee, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 30, 2003
Testing the test--why pursue a better test for Huntington disease?Reinier Timman, Anneke Maat-Kievit, Christine Brouwer-DudokdeWit, et al.
Human Genetics|September 1, 2005
Analysis of missense variants in the PKHD1-gene in patients with autosomal recessive polycystic kidney disease (ARPKD)Monique Losekoot, Cathleen Haarloo, Claudia Ruivenkamp, et al.
Pageof 12

Showing results (1-10 of 112) with videos related to

Sort By:
Pageof 12
Nederlands Tijdschrift Voor Geneeskunde|April 21, 2009
[Genetic associate studies in multifactorial genetic diseases]Martijn H Breuning
European Journal of Human Genetics : EJHG|February 24, 2005
Genetic Testing: from chromosomes to DNA, a revolution in prenatal diagnosisMartijn H Breuning
The New England Journal of Medicine|January 6, 2012
Case 26-2011: A boy with a complex kidney cystMartijn H Breuning
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2015
Response to Dalal et alKamlesh Madan, Martijn H Breuning
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 2, 2013
Impact of prenatal technologies on the sex ratio in India: an overviewKamlesh Madan, Martijn H Breuning
Methods in Cell Biology|December 18, 2004
Detecting copy number changes in genomic DNA: MAPH and MLPAStefan J White, Martijn H Breuning, Johan T den Dunnen
Pediatric Endocrinology Reviews : PER|April 28, 2009
Overgrowth syndromes:from classical to newRemco Visser, Sarina G Kant, Jan M Wit, et al.
European Journal of Human Genetics : EJHG|March 3, 2005
Unclassified variants in disease-causing genes: nonuniformity of genetic testing and counselling, a proposal for guidelinesGeraldine R Vink, Christi J van Asperen, Peter Devilee, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 30, 2003
Testing the test--why pursue a better test for Huntington disease?Reinier Timman, Anneke Maat-Kievit, Christine Brouwer-DudokdeWit, et al.
Human Genetics|September 1, 2005
Analysis of missense variants in the PKHD1-gene in patients with autosomal recessive polycystic kidney disease (ARPKD)Monique Losekoot, Cathleen Haarloo, Claudia Ruivenkamp, et al.
Pageof 12