Muller F - Search Results

1

Genetic heterogeneity between two clinical forms of cystic fibrosis evidenced by familial analysis and linked DNA probes.

Mornet E, Simon-Bouy B, Serre JL, Muller F, Taillandier A, Martinez M, Boue J, Boue A. Mornet E, et al. Among authors: muller f. Clin Genet. 1989 Feb;35(2):81-7. doi: 10.1111/j.1399-0004.1989.tb02911.x. Clin Genet. 1989. PMID: 2566403

2

Consequences of prenatal diagnosis of cystic fibrosis on the reproductive attitudes of parents of affected children.

Boué J, Muller F, Simon-Bouy B, Faure C, Boué A. Boué J, et al. Among authors: muller f. Prenat Diagn. 1991 Apr;11(4):209-14. doi: 10.1002/pd.1970110402. Prenat Diagn. 1991. PMID: 1680231

3

Intestinal dysfunction in CF affected fetuses. Results of 240 prenatal diagnoses based on microvillar enzyme activities.

Muller F, Boué J, Nezelof C, Boué A. Muller F, et al. Prog Clin Biol Res. 1987;254:191-200. Prog Clin Biol Res. 1987. PMID: 3432302 No abstract available.

4

Prenatal diagnosis in 200 pregnancies with a 1-in-4 risk of cystic fibrosis.

Boué A, Muller F, Nezelof C, Oury JF, Duchatel F, Dumez Y, Aubry MC, Boué J. Boué A, et al. Among authors: muller f. Hum Genet. 1986 Nov;74(3):288-97. doi: 10.1007/BF00282551. Hum Genet. 1986. PMID: 3536726

5

Cystic fibrosis screening: a fetus with hyperechogenic bowel may be the index case.

Muller F, Dommergues M, Simon-Bouy B, Ferec C, Oury JF, Aubry MC, Bessis R, Vuillard E, Denamur E, Bienvenu T, Serre JL. Muller F, et al. J Med Genet. 1998 Aug;35(8):657-60. doi: 10.1136/jmg.35.8.657. J Med Genet. 1998. PMID: 9719372 Free PMC article.

6

Predicting the risk of cystic fibrosis with abnormal ultrasound signs of fetal bowel: results of a French molecular collaborative study based on 641 prospective cases.

Muller F, Simon-Bouy B, Girodon E, Monnier N, Malinge MC, Serre JL; French Collaborative Group. Muller F, et al. Am J Med Genet. 2002 Jun 15;110(2):109-15. doi: 10.1002/ajmg.10431. Am J Med Genet. 2002. PMID: 12116247

7

A single chorionic gonadotropin assay for maternal serum screening for Down's syndrome.

Muller F, Boué A. Muller F, et al. Prenat Diagn. 1990 Jun;10(6):389-98. doi: 10.1002/pd.1970100606. Prenat Diagn. 1990. PMID: 2145556

8

Vasoactive intestinal peptide and its receptors in fetuses with cystic fibrosis.

Chastre E, Bawab W, Faure C, Emami S, Muller F, Boué A, Gespach C. Chastre E, et al. Among authors: muller f. Am J Physiol. 1989 Oct;257(4 Pt 1):G561-9. doi: 10.1152/ajpgi.1989.257.4.G561. Am J Physiol. 1989. PMID: 2552825

9

Prenatal diagnosis of cystic fibrosis. I. Prospective study of 51 pregnancies.

Muller F, Berg S, Frot JC, Boué J, Boué A. Muller F, et al. Prenat Diagn. 1985 Mar-Apr;5(2):97-108. doi: 10.1002/pd.1970050203. Prenat Diagn. 1985. PMID: 2581242

10

Microvillar enzyme assays in amniotic fluid and fetal tissues at different stages of development.

Muller F, Oury JF, Dumez Y, Boué J, Boué A. Muller F, et al. Prenat Diagn. 1988 Mar;8(3):189-98. doi: 10.1002/pd.1970080305. Prenat Diagn. 1988. PMID: 2897684

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