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H Scheffer

Showing results (21-30 of 154) with videos related to

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The American Journal of Gastroenterology|September 28, 2004
Relationship between partial gastric volumes and dyspeptic symptoms in fundoplication patients: a 3D ultrasonographic studyR C H Scheffer, H G Gooszen, E B Wassenaar, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
An integrated map of human chromosome 13 allowing regional localization of genetic markersR F Kooy, A Wijngaard, E Verlind, et al.
Nederlands Tijdschrift Voor Geneeskunde|November 24, 1990
[Carrier detection in relatives of patients with cystic fibrosis and their partners]L P ten Kate, H Scheffer, D J Halley, et al.
Nederlands Tijdschrift Voor Geneeskunde|August 30, 2007
[Parkinson's disease(s): recent insight into genetic factors]B P C van de Warrenburg, H Scheffer, P Heutink, et al.
Nucleic Acids Research|October 25, 1989
The anonymous probe pG50 identifying the locus D13S24 detects a two allele RFLP with SspIA M Bowcock, J M Hebert, H Scheffer, et al.
Magma (New York, N.Y.)|February 24, 2001
Use of 23Na MRS to discriminate viable from non viable tissue: experimental studiesM Horn, C Weidensteiner, H Scheffer, et al.
Nucleic Acids Research|October 25, 1989
The single copy probe pG24E2.4 [D13S21] reveals a Bsp1286 RFLP at 13q14.1-q14.2A M Bowcock, J M Hebert, H Scheffer, et al.
Human Genetics|January 1, 1991
Consanguinity sans reprocheL P Ten Kate, H Scheffer, M C Cornel, et al.
Journal of Medical Genetics|October 21, 1999
Maternal uniparental disomy for chromosome 14 in a boy with a normal karyotypeR Hordijk, H Wierenga, H Scheffer, et al.
Journal of Medical Genetics|February 5, 2002
Infantile spinal muscular atrophy variant with congenital fractures in a female neonate: evidence for autosomal recessive inheritanceW Courtens, A B Johansson, B Dachy, et al.
Pageof 16

Showing results (21-30 of 154) with videos related to

Sort By:
Pageof 16
The American Journal of Gastroenterology|September 28, 2004
Relationship between partial gastric volumes and dyspeptic symptoms in fundoplication patients: a 3D ultrasonographic studyR C H Scheffer, H G Gooszen, E B Wassenaar, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
An integrated map of human chromosome 13 allowing regional localization of genetic markersR F Kooy, A Wijngaard, E Verlind, et al.
Nederlands Tijdschrift Voor Geneeskunde|November 24, 1990
[Carrier detection in relatives of patients with cystic fibrosis and their partners]L P ten Kate, H Scheffer, D J Halley, et al.
Nederlands Tijdschrift Voor Geneeskunde|August 30, 2007
[Parkinson's disease(s): recent insight into genetic factors]B P C van de Warrenburg, H Scheffer, P Heutink, et al.
Nucleic Acids Research|October 25, 1989
The anonymous probe pG50 identifying the locus D13S24 detects a two allele RFLP with SspIA M Bowcock, J M Hebert, H Scheffer, et al.
Magma (New York, N.Y.)|February 24, 2001
Use of 23Na MRS to discriminate viable from non viable tissue: experimental studiesM Horn, C Weidensteiner, H Scheffer, et al.
Nucleic Acids Research|October 25, 1989
The single copy probe pG24E2.4 [D13S21] reveals a Bsp1286 RFLP at 13q14.1-q14.2A M Bowcock, J M Hebert, H Scheffer, et al.
Human Genetics|January 1, 1991
Consanguinity sans reprocheL P Ten Kate, H Scheffer, M C Cornel, et al.
Journal of Medical Genetics|October 21, 1999
Maternal uniparental disomy for chromosome 14 in a boy with a normal karyotypeR Hordijk, H Wierenga, H Scheffer, et al.
Journal of Medical Genetics|February 5, 2002
Infantile spinal muscular atrophy variant with congenital fractures in a female neonate: evidence for autosomal recessive inheritanceW Courtens, A B Johansson, B Dachy, et al.
Pageof 16