Pellissier MC - Search Results

1

[Balanced chromosome rearrangements with abnormal phenotype].

Philip N, Mattei MG, Pellissier MC, Mattei JF, Giraud F. Philip N, et al. Among authors: pellissier mc. J Genet Hum. 1988 Jan;36(1-2):37-43. J Genet Hum. 1988. PMID: 3379378 French.

2

[Fragile X syndrome: current knowledge].

Pellissier MC, Voelckel MA, Mattei JF. Pellissier MC, et al. Pediatrie. 1992;47(11):743-50. Pediatrie. 1992. PMID: 1364151 Review. French.

3

Prenatal diagnosis of Fryns' syndrome.

Pellissier MC, Philip N, Potier A, Scheiner C, Aymé S, Mattei JF, Giraud F. Pellissier MC, et al. Prenat Diagn. 1992 Apr;12(4):299-303. doi: 10.1002/pd.1970120410. Prenat Diagn. 1992. PMID: 1614987 Review.

4

Transmission of mental retardation with fragile X site by two normal transmitter brothers.

Pellissier MC, Voelckel MA, Piquet C, Mattei MG, Mattei JF. Pellissier MC, et al. Am J Med Genet. 1991 Feb-Mar;38(2-3):367-9. doi: 10.1002/ajmg.1320380241. Am J Med Genet. 1991. PMID: 1673312 No abstract available.

5

Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation.

Voelckel MA, Philip N, Piquet C, Pellissier MC, Oberlé I, Birg F, Mattei MG, Mattei JF. Voelckel MA, et al. Among authors: pellissier mc. Hum Genet. 1989 Mar;81(4):353-7. doi: 10.1007/BF00283690. Hum Genet. 1989. PMID: 2564838

6

Trisomy 21q223 and Down's phenotype correlation evidenced by in situ hybridization.

Pellissier MC, Laffage M, Philip N, Passage E, Mattei MG, Mattei JF. Pellissier MC, et al. Hum Genet. 1988 Nov;80(3):277-81. doi: 10.1007/BF01790097. Hum Genet. 1988. PMID: 2973430

7

Unexpected inheritance of the (CGG)n trinucleotide expansion in a fragile X syndrome family.

Malzac P, Biancalana V, Voelckel MA, Moncla A, Pellissier MC, Boccaccio I, Mattei JF. Malzac P, et al. Among authors: pellissier mc. Eur J Hum Genet. 1996;4(1):8-12. doi: 10.1159/000472163. Eur J Hum Genet. 1996. PMID: 8800930

8

Fragile X syndrome in an extended family with special reference to an affected male with Klinefelter syndrome.

Voelckel MA, Pellissier MC, Piquet C, N'Guyen C, Boccaccio I, Philip N, Mattei JF. Voelckel MA, et al. Among authors: pellissier mc. Am J Med Genet. 1991 Feb-Mar;38(2-3):374-7. doi: 10.1002/ajmg.1320380243. Am J Med Genet. 1991. PMID: 1673314

9

Fetoplacental chromosomal discrepancy.

Farra C, Giudicelli B, Pellissier MC, Philip N, Piquet C. Farra C, et al. Among authors: pellissier mc. Prenat Diagn. 2000 Mar;20(3):190-3. Prenat Diagn. 2000. PMID: 10719319

10

Prenatal and postnatal diagnosis of 22q11.2 deletion syndrome.

Bretelle F, Beyer L, Pellissier MC, Missirian C, Sigaudy S, Gamerre M, D'Ercole C, Philip N. Bretelle F, et al. Among authors: pellissier mc. Eur J Med Genet. 2010 Nov-Dec;53(6):367-70. doi: 10.1016/j.ejmg.2010.07.008. Epub 2010 Jul 24. Eur J Med Genet. 2010. PMID: 20659598

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