C M Buys - JoVE Visualize

Showing results (11-20 of 36) with videos related to

Pageof 4

Sort By:

Prenatal Diagnosis|July 6, 2006

Quality aspects of prenatal cytogenetic diagnosis: determining the effect of various factors involved in handling amniotic fluid and chorionic villus material for cytogenetic diagnosisBirgit Sikkema-Raddatz, Ron Suijkerbuijk, Katelijne Bouman, et al.

Prenatal Diagnosis|July 6, 2006

An absolute procedure to test the growth potential of medium and the influence of decreased oxygen tension in primary amniotic fluid cell culturesBirgit Sikkema-Raddatz, Ron Suijkerbuijk, Jakob van der Vlag, et al.

The Journal of Investigative Dermatology|March 29, 2002

Partial revertant mosaicism of keratin 14 in a patient with recessive epidermolysis bullosa simplexPetra H L Schuilenga-Hut, Hans Scheffer, Hendri H Pas, et al.

Scandinavian Journal of Infectious Diseases|September 5, 2003

A woman with a lobar infiltrate due to psittacosis detected by polymerase chain reactionEdou R Heddema, Maarten C Kraan, Herma E C M Buys-Bergen, et al.

Human Mutation|August 31, 2002

Occurrence of deletion of a COL2A1 allele as the mutation in Stickler syndrome shows that a collagen type II dosage effect underlies this syndromeAnnemarie H Van Der Hout, Edwin Verlind, Frits A Beemer, et al.

Human Mutation|March 26, 2003

Mutation analysis of the entire keratin 5 and 14 genes in patients with epidermolysis bullosa simplex and identification of novel mutationsPetra H L Schuilenga-Hut, Pieter v d Vlies, Marcel F Jonkman, et al.

Birth Defects Research. Part A, Clinical and Molecular Teratology|November 26, 2009

First-trimester use of paroxetine and congenital heart defects: a population-based case-control studyMarian K Bakker, Wilhelmina S Kerstjens-Frederikse, Charles H C M Buys, et al.

European Journal of Human Genetics : EJHG|May 13, 2004

Localizing a putative mutation as the major contributor to the development of sporadic Hirschsprung disease to the RET genomic sequence between the promoter region and exon 2Grzegorz M Burzynski, Ilja M Nolte, Jan Osinga, et al.

The Journal of Biological Chemistry|January 9, 2007

Ras/ERK1/2-mediated STAT3 Ser727 phosphorylation by familial medullary thyroid carcinoma-associated RET mutants induces full activation of STAT3 and is required for c-fos promoter activation, cell mitogenicity, and transformationIván Plaza-Menacho, Tineke van der Sluis, Harry Hollema, et al.

Genes, Chromosomes & Cancer|April 12, 2006

Analysis of a new homozygous deletion in the tumor suppressor region at 3p12.3 reveals two novel intronic noncoding RNA genesDebora Angeloni, Arja ter Elst, Ming Hui Wei, et al.

Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:

Pageof 4

Prenatal Diagnosis|July 6, 2006

Quality aspects of prenatal cytogenetic diagnosis: determining the effect of various factors involved in handling amniotic fluid and chorionic villus material for cytogenetic diagnosisBirgit Sikkema-Raddatz, Ron Suijkerbuijk, Katelijne Bouman, et al.

Prenatal Diagnosis|July 6, 2006

An absolute procedure to test the growth potential of medium and the influence of decreased oxygen tension in primary amniotic fluid cell culturesBirgit Sikkema-Raddatz, Ron Suijkerbuijk, Jakob van der Vlag, et al.

The Journal of Investigative Dermatology|March 29, 2002

Partial revertant mosaicism of keratin 14 in a patient with recessive epidermolysis bullosa simplexPetra H L Schuilenga-Hut, Hans Scheffer, Hendri H Pas, et al.

Scandinavian Journal of Infectious Diseases|September 5, 2003

A woman with a lobar infiltrate due to psittacosis detected by polymerase chain reactionEdou R Heddema, Maarten C Kraan, Herma E C M Buys-Bergen, et al.

Human Mutation|August 31, 2002

Occurrence of deletion of a COL2A1 allele as the mutation in Stickler syndrome shows that a collagen type II dosage effect underlies this syndromeAnnemarie H Van Der Hout, Edwin Verlind, Frits A Beemer, et al.

Human Mutation|March 26, 2003

Mutation analysis of the entire keratin 5 and 14 genes in patients with epidermolysis bullosa simplex and identification of novel mutationsPetra H L Schuilenga-Hut, Pieter v d Vlies, Marcel F Jonkman, et al.

Birth Defects Research. Part A, Clinical and Molecular Teratology|November 26, 2009

First-trimester use of paroxetine and congenital heart defects: a population-based case-control studyMarian K Bakker, Wilhelmina S Kerstjens-Frederikse, Charles H C M Buys, et al.

European Journal of Human Genetics : EJHG|May 13, 2004

Localizing a putative mutation as the major contributor to the development of sporadic Hirschsprung disease to the RET genomic sequence between the promoter region and exon 2Grzegorz M Burzynski, Ilja M Nolte, Jan Osinga, et al.

The Journal of Biological Chemistry|January 9, 2007

Ras/ERK1/2-mediated STAT3 Ser727 phosphorylation by familial medullary thyroid carcinoma-associated RET mutants induces full activation of STAT3 and is required for c-fos promoter activation, cell mitogenicity, and transformationIván Plaza-Menacho, Tineke van der Sluis, Harry Hollema, et al.

Genes, Chromosomes & Cancer|April 12, 2006

Analysis of a new homozygous deletion in the tumor suppressor region at 3p12.3 reveals two novel intronic noncoding RNA genesDebora Angeloni, Arja ter Elst, Ming Hui Wei, et al.

Pageof 4