Boue J - Search Results

1

Prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia by simultaneous radioimmunoassay of 21-deoxycortisol and 17-hydroxyprogesterone in amniotic fluid.

Gueux B, Fiet J, Couillin P, Raux-Demay MC, Mornet E, Galons H, Villette JM, Boue J, Dreux C. Gueux B, et al. Among authors: boue j. J Clin Endocrinol Metab. 1988 Mar;66(3):534-7. doi: 10.1210/jcem-66-3-534. J Clin Endocrinol Metab. 1988. PMID: 3258316

2

Early prenatal diagnosis of 21-hydroxylase deficiency using amniotic fluid 17-hydroxyprogesterone determination and DNA probes.

Raux-Demay M, Mornet E, Boue J, Couillin P, Oury JF, Ravise N, Deluchat C, Boue A. Raux-Demay M, et al. Among authors: boue a, boue j. Prenat Diagn. 1989 Jul;9(7):457-66. doi: 10.1002/pd.1970090702. Prenat Diagn. 1989. PMID: 2788885

3

[Current data on the molecular biology of 21-hydroxylase deficiency. Diagnostic applications].

Mornet E, Boué J, Crète P, Raux-Demay MC, Kutten F, Boué A. Mornet E, et al. Among authors: boue a, boue j. Arch Fr Pediatr. 1992 Jan;49(1):57-62. Arch Fr Pediatr. 1992. PMID: 1550455 French. No abstract available.

4

Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiency.

Mornet E, Crété P, Kuttenn F, Raux-Demay MC, Boué J, White PC, Boué A. Mornet E, et al. Among authors: boue a, boue j. Am J Hum Genet. 1991 Jan;48(1):79-88. Am J Hum Genet. 1991. PMID: 1985465 Free PMC article.

5

First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination.

Mornet E, Boue J, Raux-Demay M, Couillin P, Oury JF, Dumez Y, Dausset J, Cohen D, Boué A. Mornet E, et al. Among authors: boue a, boue j. Hum Genet. 1986 Aug;73(4):358-64. doi: 10.1007/BF00279101. Hum Genet. 1986. PMID: 3017844

6

Prenatal diagnosis of congenital adrenal hyperplasia (21-OH deficiency type) by HLA typing.

Couillin P, Boue J, Nicolas H, Cheruy C, Boue A. Couillin P, et al. Among authors: boue a, boue j. Prenat Diagn. 1981 Jan;1(1):25-33. doi: 10.1002/pd.1970010107. Prenat Diagn. 1981. PMID: 6955777

7

Screening of CYP21 gene mutations in 129 French patients affected by steroid 21-hydroxylase deficiency.

Barbat B, Bogyo A, Raux-Demay MC, Kuttenn F, Boué J, Simon-Bouy B, Serre JL, Mornet E. Barbat B, et al. Among authors: boue j. Hum Mutat. 1995;5(2):126-30. doi: 10.1002/humu.1380050205. Hum Mutat. 1995. PMID: 7749410

8

[Genetic of the 21 hydroxylase deficiency].

Boué A, Couillin P, Pomarède R, Rappaport R, Boué J. Boué A, et al. Among authors: boue j. Ann Endocrinol (Paris). 1982;43(1):3-14. Ann Endocrinol (Paris). 1982. PMID: 6982657 French.

9

[Congenital adrenal hyperplasia and HLA antigens].

Boué A, Boué J, Couillin P. Boué A, et al. Among authors: boue j. J Genet Hum. 1980 Sep;28(3):195-200. J Genet Hum. 1980. PMID: 7463017 French. No abstract available.

10

HLA typing of amniotic-fluid cells applied to prenatal diagnosis of congenital adrenal hyperplasia.

Couillin P, Nicolas H, Boué J, Boué A. Couillin P, et al. Among authors: boue a, boue j. Lancet. 1979 May 19;1(8125):1076. doi: 10.1016/s0140-6736(79)92966-0. Lancet. 1979. PMID: 86789 No abstract available.

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