Piquet C - Search Results

1

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: piquet c. Am J Med Genet. 1991 Feb-Mar;38(2-3):374-7. doi: 10.1002/ajmg.1320380243. Am J Med Genet. 1991. PMID: 1673314

2

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. Among authors: piquet c. 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.

3

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: piquet c. Hum Genet. 1989 Mar;81(4):353-7. doi: 10.1007/BF00283690. Hum Genet. 1989. PMID: 2564838

4

Fetoplacental chromosomal discrepancy.

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

5

Prenatal diagnosis of 22q11 microdeletion.

Levy-Mozziconacci A, Piquet C, Heurtevin PC, Philip N. Levy-Mozziconacci A, et al. Among authors: piquet c. Prenat Diagn. 1997 Nov;17(11):1033-7. Prenat Diagn. 1997. PMID: 9399351 Clinical Trial.

6

Prenatal ultrasonographic findings in Proteus syndrome.

Sigaudy S, Fredouille C, Gambarelli D, Potier A, Cassin D, Piquet C, Philip N. Sigaudy S, et al. Among authors: piquet c. Prenat Diagn. 1998 Oct;18(10):1091-4. Prenat Diagn. 1998. PMID: 9826904

7

Congenital bowing of long bones: prenatal ultrasound findings and diagnostic dilemmas.

Farra C, Piquet C, Guillaume M, D'Ercole C, Philip N. Farra C, et al. Among authors: piquet c. Fetal Diagn Ther. 2002 Jul-Aug;17(4):236-9. doi: 10.1159/000059376. Fetal Diagn Ther. 2002. PMID: 12065952

8

i(18q) in amniotic and fetal cells with a normal karyotype in direct chorionic villus sampling: cytogenetics and pathology.

Levy-Mozziconacci A, Piquet C, Scheiner C, Adrai J, Potier A, Pelissier MC, Philip N. Levy-Mozziconacci A, et al. Among authors: piquet c. Prenat Diagn. 1996 Dec;16(12):1156-9. doi: 10.1002/(SICI)1097-0223(199612)16:12<1156::AID-PD13>3.0.CO;2-K. Prenat Diagn. 1996. PMID: 8994254

9

Fetal karyotype from cystic hygroma fluid: diploid/tetraploid mosaicism.

Piquet C, Gamerre M, Levy A, Scheiner C, Philip N. Piquet C, et al. Prenat Diagn. 1993 Aug;13(8):770-1. doi: 10.1002/pd.1970130813. Prenat Diagn. 1993. PMID: 8123164 No abstract available.

10

[Chorionic villus needle sampling by the transabdominal route or by placental centesis. A series of 930 cases].

Guidicelli B, Levy A, Piquet C, Gamerre M. Guidicelli B, et al. Among authors: piquet c. J Gynecol Obstet Biol Reprod (Paris). 1993;22(8):851-5. J Gynecol Obstet Biol Reprod (Paris). 1993. PMID: 8132961 French.

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