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[Prenatal diagnosis of various hereditary blinding diseases].
Michel-Awad A, Kaplan J, Briard ML, Turleau C, de Grouchy J, Munnich A, Dufier JL, Frezal J. Michel-Awad A, et al. Among authors: de grouchy j. Ophtalmologie. 1990 May-Jun;4(3):237-9. Ophtalmologie. 1990. PMID: 2250955 French.
6q1 monosomy: a distinctive syndrome.
Turleau C, Demay G, Cabanis MO, Lenoir G, de Grouchy J. Turleau C, et al. Among authors: de grouchy j. Clin Genet. 1988 Jul;34(1):38-42. doi: 10.1111/j.1399-0004.1988.tb02613.x. Clin Genet. 1988. PMID: 3409537
Microcytogenetics 1984.
de Grouchy J, Turleau C. de Grouchy J, et al. Experientia. 1986 Oct 15;42(10):1090-7. doi: 10.1007/BF01941282. Experientia. 1986. PMID: 3533601 Review. No abstract available.
Trisomy 18qter and trisomy mapping of chromosome 18.
Turleau C, de Grouchy J. Turleau C, et al. Among authors: de grouchy j. Clin Genet. 1977 Dec;12(6):361-71. doi: 10.1111/j.1399-0004.1977.tb00955.x. Clin Genet. 1977. PMID: 589857 No abstract available.
328 results