Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

S Gilgenkrantz

Showing results (71-80 of 129) with videos related to

Pageof 13
Sort By:
Journal De Genetique Humaine|September 1, 1981
[Hallervorden-Spatz familial dystonia apropos of a family in which 3 brothers are afflicted. Diagnostic and genetic discussion]F Cruz-Marin, M Gerard, O Brocard, et al.
Journal De Genetique Humaine|March 1, 1981
[Linkage between congenital adrenal hyperplasia with 21-hydroxylase deficiency and HLA histocompatibility groups]F Cruz-Marin, C Raffoux, S Gilgenkrantz, 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|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.
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.
American Journal of Medical Genetics|February 11, 1997
Autosomal recessive lateralization and midline defects: blastogenesis recessive 1S Debrus, U Sauer, S Gilgenkrantz, et al.
Human Genetics|January 1, 1981
Duplication 15q22 to 15qter and its phenotypic expressionM J Gregoire, J Boue, C Junien, 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.
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.
Pageof 13

Showing results (71-80 of 129) with videos related to

Sort By:
Pageof 13
Journal De Genetique Humaine|September 1, 1981
[Hallervorden-Spatz familial dystonia apropos of a family in which 3 brothers are afflicted. Diagnostic and genetic discussion]F Cruz-Marin, M Gerard, O Brocard, et al.
Journal De Genetique Humaine|March 1, 1981
[Linkage between congenital adrenal hyperplasia with 21-hydroxylase deficiency and HLA histocompatibility groups]F Cruz-Marin, C Raffoux, S Gilgenkrantz, 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|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.
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.
American Journal of Medical Genetics|February 11, 1997
Autosomal recessive lateralization and midline defects: blastogenesis recessive 1S Debrus, U Sauer, S Gilgenkrantz, et al.
Human Genetics|January 1, 1981
Duplication 15q22 to 15qter and its phenotypic expressionM J Gregoire, J Boue, C Junien, 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.
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.
Pageof 13