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I B Van den Veyver

Showing results (1-10 of 35) with videos related to

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Cytogenetic and Genome Research|August 6, 2003
Microphthalmia with linear skin defects (MLS), Aicardi, and Goltz syndromes: are they related X-linked dominant male-lethal disorders?I B Van den Veyver
Seminars in Reproductive Medicine|August 2, 2001
Skewed X inactivation in X-linked disordersI B Van den Veyver
Current Opinion in Genetics & Development|May 29, 2000
Methyl-CpG-binding protein 2 mutations in Rett syndromeI B Van den Veyver, H Y Zoghbi
Obstetrical & Gynecological Survey|July 1, 1993
Prostaglandin synthetase inhibitors in pregnancyI B Van den Veyver, K J Moise
Current Opinion in Obstetrics & Gynecology|April 29, 1998
Applied molecular genetic techniques for prenatal diagnosisI B Van den Veyver, B B Roa
Obstetrics and Gynecology|December 1, 1996
Fetal RhD typing by polymerase chain reaction in pregnancies complicated by rhesus alloimmunizationI B Van den Veyver, K J Moise
Brain & Development|December 12, 2001
Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndromeI B Van den Veyver, H Y Zoghbi
Human Reproduction Update|March 17, 2006
Biparental hydatidiform moles: a maternal effect mutation affecting imprinting in the offspringI B Van den Veyver, T K Al-Hussaini
Clinics in Perinatology|September 1, 1994
Treatment of polyhydramnios with indomethacinW B Kramer, I B Van den Veyver, B Kirshon
American Journal of Medical Genetics|July 23, 1998
Genomic structure of a human holocytochrome c-type synthetase gene in Xp22.3 and mutation analysis in patients with Rett syndromeI B Van den Veyver, S Subramanian, H Y Zoghbi
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Cytogenetic and Genome Research|August 6, 2003
Microphthalmia with linear skin defects (MLS), Aicardi, and Goltz syndromes: are they related X-linked dominant male-lethal disorders?I B Van den Veyver
Seminars in Reproductive Medicine|August 2, 2001
Skewed X inactivation in X-linked disordersI B Van den Veyver
Current Opinion in Genetics & Development|May 29, 2000
Methyl-CpG-binding protein 2 mutations in Rett syndromeI B Van den Veyver, H Y Zoghbi
Obstetrical & Gynecological Survey|July 1, 1993
Prostaglandin synthetase inhibitors in pregnancyI B Van den Veyver, K J Moise
Current Opinion in Obstetrics & Gynecology|April 29, 1998
Applied molecular genetic techniques for prenatal diagnosisI B Van den Veyver, B B Roa
Obstetrics and Gynecology|December 1, 1996
Fetal RhD typing by polymerase chain reaction in pregnancies complicated by rhesus alloimmunizationI B Van den Veyver, K J Moise
Brain & Development|December 12, 2001
Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndromeI B Van den Veyver, H Y Zoghbi
Human Reproduction Update|March 17, 2006
Biparental hydatidiform moles: a maternal effect mutation affecting imprinting in the offspringI B Van den Veyver, T K Al-Hussaini
Clinics in Perinatology|September 1, 1994
Treatment of polyhydramnios with indomethacinW B Kramer, I B Van den Veyver, B Kirshon
American Journal of Medical Genetics|July 23, 1998
Genomic structure of a human holocytochrome c-type synthetase gene in Xp22.3 and mutation analysis in patients with Rett syndromeI B Van den Veyver, S Subramanian, H Y Zoghbi
Pageof 4