Debost-Legrand A - Search Results

1

Prenatal ultrasound findings observed in the Wolf-Hirschhorn syndrome: data from the registry of congenital malformations in Auvergne.

Debost-Legrand A, Goumy C, Laurichesse-Delmas H, Déchelotte P, Beaufrère AM, Lémery D, Francannet C, Gallot D. Debost-Legrand A, et al. Birth Defects Res A Clin Mol Teratol. 2013 Dec;97(12):806-11. doi: 10.1002/bdra.23194. Epub 2013 Nov 6. Birth Defects Res A Clin Mol Teratol. 2013. PMID: 24343879

2

Prenatal detection of cryptic rearrangements by multiplex ligation probe amplification in fetuses with ultrasound abnormalities.

Goumy C, Gouas L, Pebrel-Richard C, Véronèse L, Eymard-Pierre E, Debost-Legrand A, Haoud K, Tchirkov A, Vago P. Goumy C, et al. Genet Med. 2010 Jun;12(6):376-80. doi: 10.1097/GIM.0b013e3181e074c6. Genet Med. 2010. PMID: 20453657 Free article.

3

De novo unbalanced translocation 2;4 characterized by metaphase CGH and array CGH in a child with mental retardation and dysmorphic features.

Debost-Legrand A, Capri Y, Gouas L, Pebrel-Richard C, Veronese L, Tchirkov A, Haoud K, Boespflug-Tanguy O, Goumy C, Vago P. Debost-Legrand A, et al. Pathol Biol (Paris). 2011 Dec;59(6):309-13. doi: 10.1016/j.patbio.2010.11.004. Epub 2010 Dec 9. Pathol Biol (Paris). 2011. PMID: 21145667

4

A new case of 8q22.1 microdeletion restricts the critical region for Nablus mask-like facial syndrome.

Debost-Legrand A, Eymard-Pierre E, Pebrel-Richard C, Gouas L, Goumy C, Giollant M, Ayed W, Tchirkov A, Francannet C, Vago P. Debost-Legrand A, et al. Am J Med Genet A. 2013 Jan;161A(1):162-5. doi: 10.1002/ajmg.a.35614. Epub 2012 Dec 13. Am J Med Genet A. 2013. PMID: 23239647

5

A new mutation that predicted a drastic alteration of the BTK protein function.

Debost-Legrand A, Legrand G, Moulillot G, Francannet C, Bocly B, Theodoroub I, Paillard C. Debost-Legrand A, et al. Gene. 2013 Sep 15;527(1):426-8. doi: 10.1016/j.gene.2013.05.070. Epub 2013 Jun 15. Gene. 2013. PMID: 23774691

6

An unusual clinical severity of 16p11.2 deletion syndrome caused by unmasked recessive mutation of CLN3.

Pebrel-Richard C, Debost-Legrand A, Eymard-Pierre E, Greze V, Kemeny S, Gay-Bellile M, Gouas L, Tchirkov A, Vago P, Goumy C, Francannet C. Pebrel-Richard C, et al. Eur J Hum Genet. 2014 Mar;22(3):369-73. doi: 10.1038/ejhg.2013.141. Epub 2013 Jul 17. Eur J Hum Genet. 2014. PMID: 23860047 Free PMC article.

7

False positive morphologic diagnoses at the anomaly scan: marginal or real problem, a population-based cohort study.

Debost-Legrand A, Laurichesse-Delmas H, Francannet C, Perthus I, Lémery D, Gallot D, Vendittelli F. Debost-Legrand A, et al. BMC Pregnancy Childbirth. 2014 Mar 24;14:112. doi: 10.1186/1471-2393-14-112. BMC Pregnancy Childbirth. 2014. PMID: 24655605 Free PMC article.

8

Severe secondary postpartum hemorrhage: a historical cohort.

Dossou M, Debost-Legrand A, Déchelotte P, Lémery D, Vendittelli F. Dossou M, et al. Birth. 2015 Jun;42(2):149-55. doi: 10.1111/birt.12164. Epub 2015 Apr 13. Birth. 2015. PMID: 25867033

9

Prenatal diagnosis of the VACTERL association using routine ultrasound examination.

Debost-Legrand A, Goumy C, Laurichesse-Delmas H, Déchelotte P, Perthus I, Francannet C, Lémery D, Gallot D. Debost-Legrand A, et al. Birth Defects Res A Clin Mol Teratol. 2015 Oct;103(10):880-6. doi: 10.1002/bdra.23346. Epub 2015 Jun 2. Birth Defects Res A Clin Mol Teratol. 2015. PMID: 26033534

10

Reliability of student midwives' visual estimate of blood loss in the immediate postpartum period: a cross-sectional study.

Parayre I, Rivière O, Debost-Legrand A, Lémery D, Vendittelli F. Parayre I, et al. Int J Nurs Stud. 2015 Dec;52(12):1798-803. doi: 10.1016/j.ijnurstu.2015.06.015. Epub 2015 Jul 3. Int J Nurs Stud. 2015. PMID: 26233835

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