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Annales De Genetique|January 1, 1985
Translocation (X;9)(p11;q34) in a girl with incontinentia pigmenti (IP): implications for the regional assignment of the IP locus to Xp11?S Gilgenkrantz, P Tridon, N Pinel-Briquel, et al.Journal De Genetique Humaine|June 1, 1985
[Prenatal diagnosis of triploidy. I. Echographic, clinical and anatomic studies]S Gilgenkrantz, P Droulle, M Schweitzer, et al.Journal De Genetique Humaine|December 1, 1980
[Phenotype of a ring-chromosome 6 carrier. Clinical and cytogenetic study]F Cruz-Marin, S Gilgenkrantz, M J Gregoire, et al.American Journal of Clinical Pathology|March 1, 1990
Use of Gen-Probe and Bactec for rapid isolation and identification of mycobacteria. Correlation of probe results with growth indexB A Body, N G Warren, A Spicer, 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.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 24