Beaujard MP - Search Results

1

Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.

Beaujard MP, Jouannic JM, Bessières B, Borie C, Martin-Luis I, Fallet-Bianco C, Portnoï MF. Beaujard MP, et al. Prenat Diagn. 2005 Jun;25(6):451-5. doi: 10.1002/pd.1154. Prenat Diagn. 2005. PMID: 15966060

2

[Abnormal placental caryotype in severe intrauterine growth retardations (IUGR). Case report].

Colmant C, Mirlesse V, Beaujard MP, Bessières B, Daffos F. Colmant C, et al. Among authors: beaujard mp. Gynecol Obstet Fertil. 2007 Sep;35(9):780-4. doi: 10.1016/j.gyobfe.2007.05.020. Epub 2007 Aug 17. Gynecol Obstet Fertil. 2007. PMID: 17707675 French.

3

Very elevated hCGβ (≥10 multiple of the median) in maternal marker screening for Down syndrome: Frequency, etiologies, outcomes, and guidelines.

Dreux S, Rosenblatt J, Massardier J, Benachi A, Voirin-Mathieu E; ABA Study Group; Muller F. Dreux S, et al. Prenat Diagn. 2024 Jul;44(8):959-964. doi: 10.1002/pd.6588. Epub 2024 May 17. Prenat Diagn. 2024. PMID: 38757850

4

[First trimester screening for Down syndrome at Prima facie. A 6-year survey].

Roth P, Bernard JP, Meyer V, Beaujard MP, Salomon LJ, Ville Y. Roth P, et al. Among authors: beaujard mp. Gynecol Obstet Fertil. 2016 Feb;44(2):101-5. doi: 10.1016/j.gyobfe.2015.11.009. Epub 2015 Dec 22. Gynecol Obstet Fertil. 2016. PMID: 26725884 French.

5

[Down syndrome maternal serum screening: results' comments recommended by accredited biologists].

Muller F, Dreux S, Czerkiewicz I, Bernard M, Guibourdenche J, Lacroix I, Moineau MP, Read MH, Sault C, Thibaud D, Veyrat B; ABA; Bidat L. Muller F, et al. J Gynecol Obstet Biol Reprod (Paris). 2014 Nov;43(9):671-9. doi: 10.1016/j.jgyn.2014.05.012. Epub 2014 Sep 11. J Gynecol Obstet Biol Reprod (Paris). 2014. PMID: 25218268 French.

6

Down syndrome maternal serum marker screening after 18 weeks of gestation: a countrywide study.

Dreux S, Nguyen C, Czerkiewicz I, Schmitz T, Azria E, Fouré MA, Muller F; ABA Study Group. Dreux S, et al. Am J Obstet Gynecol. 2013 May;208(5):397.e1-5. doi: 10.1016/j.ajog.2013.01.039. Epub 2013 Jan 24. Am J Obstet Gynecol. 2013. PMID: 23353023

7

Expanding the phenotypic spectrum of LIG4 pathogenic variations: neuro-histopathological description of 4 fetuses with stenosis of the aqueduct.

Nicolle R, Boutaud L, Loeuillet L, Talhi N, Grotto S, Bourgon N, Feresin A, Coussement A, Barrois M, Beaujard MP, Rambaud T, Razavi F, Attié-Bitach T. Nicolle R, et al. Among authors: beaujard mp. Eur J Hum Genet. 2024 May;32(5):545-549. doi: 10.1038/s41431-024-01558-2. Epub 2024 Feb 13. Eur J Hum Genet. 2024. PMID: 38351293

8

Hydrothorax in fetal cases of Opitz G/BBB diagnosis: Extending the phenotype?

Tessier A, Boutaud L, Bruel AL, Thauvin-Robinet C, Roth P, Malan V, Beaujard MP, Achaiaa A, de Oliveira J, Steffann J, Encha-Razavi F, Faivre L, Bessières B, Attié-Bitach T. Tessier A, et al. Among authors: beaujard mp. Clin Genet. 2020 Dec;98(6):620-621. doi: 10.1111/cge.13840. Epub 2020 Sep 14. Clin Genet. 2020. PMID: 32926417

9

A French Approach to Test Fetuses with Ultrasound Abnormalities Using a Customized Microarray as First-Tier Genetic Test.

Malan V, Lapierre JM, Egloff M, Goidin D, Beaujard MP, Maurin ML, Attié-Bitach T, Bessières B, Bernard JP, Roth P, Stirnemann J, Salomon L, Romana S, Vekemans M, Ville Y, Turleau C. Malan V, et al. Among authors: beaujard mp. Cytogenet Genome Res. 2015;147(2-3):103-10. doi: 10.1159/000442904. Epub 2016 Jan 7. Cytogenet Genome Res. 2015. PMID: 26735902

10

First-trimester combined screening for trisomy 21 in women with renal disease.

Valentin M, Muller F, Beaujard MP, Dreux S, Czerkiewicz I, Meyer V, Leruez M, Ville Y, Salomon LJ. Valentin M, et al. Among authors: beaujard mp. Prenat Diagn. 2015 Mar;35(3):244-8. doi: 10.1002/pd.4528. Epub 2015 Feb 2. Prenat Diagn. 2015. PMID: 25395363

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