Philip N - Search Results

1

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: philip n. Prenat Diagn. 1998 Oct;18(10):1091-4. Prenat Diagn. 1998. PMID: 9826904

2

Prenatal diagnosis of Fryns' syndrome.

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

3

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

4

Holoprosencephaly-polydactyly ('pseudotrisomy 13') syndrome: a syndrome with features of hydrolethalus and Smith-Lemli-Opitz syndromes. A collaborative multicentre study.

Verloes A, Aymé S, Gambarelli D, Gonzales M, Le Merrer M, Mulliez N, Philip N, Roume J. Verloes A, et al. Among authors: philip n. J Med Genet. 1991 May;28(5):297-303. doi: 10.1136/jmg.28.5.297. J Med Genet. 1991. PMID: 1865466 Free PMC article. Review.

5

Epidemiological study of congenital diaphragmatic defects with special reference to aetiology.

Philip N, Gambarelli D, Guys JM, Camboulives J, Ayme S. Philip N, et al. Eur J Pediatr. 1991 Aug;150(10):726-9. doi: 10.1007/BF01958765. Eur J Pediatr. 1991. PMID: 1915486

6

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

7

Fryns syndrome: report on 8 new cases.

Aymé S, Julian C, Gambarelli D, Mariotti B, Luciani A, Sudan N, Maurin N, Philip N, Serville F, Carles D, et al. Aymé S, et al. Among authors: philip n. Clin Genet. 1989 Mar;35(3):191-201. doi: 10.1111/j.1399-0004.1989.tb02927.x. Clin Genet. 1989. PMID: 2650934 Review.

8

Fetal abnormalities detected by sonography in low-risk pregnancies: discrepancies between pre- and post-termination findings.

Julian-Reynier C, Macquart-Moulin G, Philip N, Scheiner C, Potier A, Gambarelli D, Aymé S. Julian-Reynier C, et al. Among authors: philip n. Fetal Diagn Ther. 1994 Sep-Oct;9(5):310-20. doi: 10.1159/000263954. Fetal Diagn Ther. 1994. PMID: 7818779

9

Impact of prenatal diagnosis by ultrasound on the prevalence of congenital anomalies at birth in southern France.

Julian-Reynier C, Philip N, Scheiner C, Aurran Y, Chabal F, Maron A, Gombert A, Aymé S. Julian-Reynier C, et al. Among authors: philip n. J Epidemiol Community Health. 1994 Jun;48(3):290-6. doi: 10.1136/jech.48.3.290. J Epidemiol Community Health. 1994. PMID: 8051530 Free PMC article.

10

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

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

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