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Gilgenkrantz

Showing results (101-110 of 233) with videos related to

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Journal De Genetique Humaine|January 1, 1987
[Mosaic tetrasomy 12p. Identical nature of the Pallister syndrome, the Teschler-Nicola/Killian syndrome and mosaic tetrasomy 21]S Gilgenkrantz, J P Fryns, P Droulle, et al.
Human Genetics|October 1, 1988
Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal markerA Hanauer, Y Alembik, B Arveiler, et al.
Human Genetics|January 1, 1989
Hypohidrotic ectodermal dysplasia. Clinical study of a family of 30 over three generationsS Gilgenkrantz, C Blanchet-Bardon, V Nazzaro, et al.
Journal De Genetique Humaine|August 1, 1986
[Unexpected chromosomal abnormalities in prenatal diagnosis. 4 case reports with preservation of the pregnancy]S Gilgenkrantz, M Schweitzer, P Droulle, et al.
Revue De Pneumologie Clinique|January 1, 1985
[The scimitar sign: a pulmonary vein or systemic artery? Apropos of a case of pure vascular sequestration]K Khalife, N Sadoul, J Fays, et al.
American Journal of Medical Genetics|February 11, 1997
Autosomal recessive lateralization and midline defects: blastogenesis recessive 1S Debrus, U Sauer, S Gilgenkrantz, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1975
[Pre-hospital resuscitation and transport of cardiac patients. Apropos of 107 cases of primary transport]J M Gilgenkrantz, A Larcan, M C Laprevotte, et al.
Journal of Medical Genetics|December 1, 1981
Partial proximal trisomy of the long arm of chromosome 5 (q13 leads to q22) resulting from maternal insertion der ins (10;5)S Gilgenkrantz, P Dulucq, J L Bresson, et al.
Human Genetics|September 1, 1992
Linkage study in a large pedigree with Stickler syndrome: exclusion of COL2A1 as the mutant geneJ Bonaventure, C Philippe, G Plessis, et al.
The American Journal of Pathology|January 12, 2002
Liver repopulation by Bcl-x(L) transgenic hepatocytesClaudia Mitchell, Vincent O Mallet, Jacques E Guidotti, et al.
Pageof 24

Showing results (101-110 of 233) with videos related to

Sort By:
Pageof 24
Journal De Genetique Humaine|January 1, 1987
[Mosaic tetrasomy 12p. Identical nature of the Pallister syndrome, the Teschler-Nicola/Killian syndrome and mosaic tetrasomy 21]S Gilgenkrantz, J P Fryns, P Droulle, et al.
Human Genetics|October 1, 1988
Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal markerA Hanauer, Y Alembik, B Arveiler, et al.
Human Genetics|January 1, 1989
Hypohidrotic ectodermal dysplasia. Clinical study of a family of 30 over three generationsS Gilgenkrantz, C Blanchet-Bardon, V Nazzaro, et al.
Journal De Genetique Humaine|August 1, 1986
[Unexpected chromosomal abnormalities in prenatal diagnosis. 4 case reports with preservation of the pregnancy]S Gilgenkrantz, M Schweitzer, P Droulle, et al.
Revue De Pneumologie Clinique|January 1, 1985
[The scimitar sign: a pulmonary vein or systemic artery? Apropos of a case of pure vascular sequestration]K Khalife, N Sadoul, J Fays, et al.
American Journal of Medical Genetics|February 11, 1997
Autosomal recessive lateralization and midline defects: blastogenesis recessive 1S Debrus, U Sauer, S Gilgenkrantz, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1975
[Pre-hospital resuscitation and transport of cardiac patients. Apropos of 107 cases of primary transport]J M Gilgenkrantz, A Larcan, M C Laprevotte, et al.
Journal of Medical Genetics|December 1, 1981
Partial proximal trisomy of the long arm of chromosome 5 (q13 leads to q22) resulting from maternal insertion der ins (10;5)S Gilgenkrantz, P Dulucq, J L Bresson, et al.
Human Genetics|September 1, 1992
Linkage study in a large pedigree with Stickler syndrome: exclusion of COL2A1 as the mutant geneJ Bonaventure, C Philippe, G Plessis, et al.
The American Journal of Pathology|January 12, 2002
Liver repopulation by Bcl-x(L) transgenic hepatocytesClaudia Mitchell, Vincent O Mallet, Jacques E Guidotti, et al.
Pageof 24