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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 2
2005 1
2006 4
2007 6
2008 5
2009 5
2010 7
2011 4
2012 7
2013 11
2014 10
2015 14
2016 8
2017 8
2018 6
2019 13
2020 2
2021 7
2022 8
2023 6
2024 2

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112 results

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Egloff M, Malan V. Egloff M, et al. Among authors: malan v. Ultrasound Obstet Gynecol. 2019 Apr;53(4):555. doi: 10.1002/uog.20253. Ultrasound Obstet Gynecol. 2019. PMID: 30938480 Free article. No abstract available.
[Cell-free fetal DNA screening tests for trisomy 21].
Malan V, Bussières L, Salomon LJ. Malan V, et al. Gynecol Obstet Fertil. 2016 Dec;44(12):675-678. doi: 10.1016/j.gyobfe.2016.10.002. Epub 2016 Nov 7. Gynecol Obstet Fertil. 2016. PMID: 27839716 Review. French. No abstract available.
Chimera and other fertilization errors.
Malan V, Vekemans M, Turleau C. Malan V, et al. Clin Genet. 2006 Nov;70(5):363-73. doi: 10.1111/j.1399-0004.2006.00689.x. Clin Genet. 2006. PMID: 17026615 Review.
[Managing and identifying the causes of IUGR].
Salomon LJ, Malan V. Salomon LJ, et al. Among authors: malan v. J Gynecol Obstet Biol Reprod (Paris). 2013 Dec;42(8):929-40. doi: 10.1016/j.jgyn.2013.09.016. Epub 2013 Nov 7. J Gynecol Obstet Biol Reprod (Paris). 2013. PMID: 24210716 Free article. Review. French.
Retrospective evaluation of clinical and molecular data of 148 cases of esophageal atresia.
Ranza E, Le Gouez M, Guimier A, Dunlop NK, Beaudoin S, Malan V, Michot C, Baujat G, Rio M, Cormier-Daire V, Abadie V, Sarnacki S, Delacourt C, Lyonnet S, Attié-Bitach T, Pingault V, Rousseau V, Amiel J. Ranza E, et al. Among authors: malan v. Am J Med Genet A. 2023 Jan;191(1):77-83. doi: 10.1002/ajmg.a.62989. Epub 2022 Oct 21. Am J Med Genet A. 2023. PMID: 36271508
Ellis-Van Creveld Syndrome: Clinical and Molecular Analysis of 50 Individuals.
Aubert-Mucca M, Huber C, Baujat G, Michot C, Zarhrate M, Bras M, Boutaud L, Malan V, Attie-Bitach T; Clinical Contributors; Cormier-Daire V. Aubert-Mucca M, et al. Among authors: malan v. J Med Genet. 2023 Apr;60(4):337-345. doi: 10.1136/jmg-2022-108435. Epub 2022 Aug 4. J Med Genet. 2023. PMID: 35927022
Prenatal findings in 1p36 deletion syndrome: New cases and a literature review.
Guterman S, Beneteau C, Redon S, Dupont C, Missirian C, Jaeger P, Herve B, Jacquin C, Douet-Guilbert N, Till M, Tabet AC, Moradkhani K, Malan V, Doco-Fenzy M, Vialard F. Guterman S, et al. Among authors: malan v. Prenat Diagn. 2019 Sep;39(10):871-882. doi: 10.1002/pd.5498. Epub 2019 Jul 5. Prenat Diagn. 2019. PMID: 31172545 Review.
Antenatal ultrasound features of isolated recurrent copy number variation in 7q11.23 (Williams syndrome and 7q11.23 duplication syndrome).
Courdier C, Boudjarane J, Malan V, Muti C, Sperelakis-Beedham B, Odent S, Jaillard S, Quelin C, Le Caignec C, Patat O, Dubucs C, Julia S, Schluth-Bolard C, Goumy C, Redon S, Gaillard JB, Huynh MT, Dupont C, Tabet AC, Cogan G, Vialard F, Dard R, Jedraszak G, Jobic F, Lefebvre M, Quenum G, Inai S, Rama M, Sauvestre F, Coatleven F, Thomas J, Rooryck C. Courdier C, et al. Among authors: malan v. Prenat Diagn. 2023 Jun;43(6):734-745. doi: 10.1002/pd.6340. Epub 2023 Mar 23. Prenat Diagn. 2023. PMID: 36914926 Free article.
Phenotype-genotype correlations in 17 new patients with an Xp11.23p11.22 microduplication and review of the literature.
Nizon M, Andrieux J, Rooryck C, de Blois MC, Bourel-Ponchel E, Bourgois B, Boute O, David A, Delobel B, Duban-Bedu B, Giuliano F, Goldenberg A, Grotto S, Héron D, Karmous-Benailly H, Keren B, Lacombe D, Lapierre JM, Le Caignec C, Le Galloudec E, Le Merrer M, Le Moing AG, Mathieu-Dramard M, Nusbaum S, Pichon O, Pinson L, Raoul O, Rio M, Romana S, Roubertie A, Colleaux L, Turleau C, Vekemans M, Nabbout R, Malan V. Nizon M, et al. Among authors: malan v. Am J Med Genet A. 2015 Jan;167A(1):111-22. doi: 10.1002/ajmg.a.36807. Epub 2014 Nov 25. Am J Med Genet A. 2015. PMID: 25425167 Review.
112 results