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American Journal of Medical Genetics|April 12, 2001
Problems in the diagnosis of fragile X syndrome in young children are still presentC StollGenetic Counseling (Geneva, Switzerland)|August 2, 2002
Pseudoachondroplasia with cerebral and renal cystsC StollPathologie-Biologie|November 1, 1982
[Chromosomal abnormalities of the blastic phase of chronic myeloid leukemia]C StollGenetic Counseling (Geneva, Switzerland)|January 13, 2000
Congenital blepharophimosis and ptosis in a mentally retarded girl: a new case of Ohdo syndrome?C StollHuman Genetics|January 1, 1980
Nonrandom distribution of exchange points in patients with reciprocal translocationsC StollGenetic Counseling (Geneva, Switzerland)|July 23, 2003
Macrocephaly-cutis marmorata telangiectatica congenita: report of a patient with a translocationC StollHuman 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.Pediatrie|September 1, 1985
[Opsomyoclonus syndrome in children. A new case. Review of the literature (110 cases)]P Talon, C StollPageof 30