Baumann C - Search Results

1

Aphallia, lung agenesis and multiple defects of blastogenesis.

Gérard-Blanluet M, Lambert V, Khung-Savatovsky S, Perrin-Sabourin L, Passemard S, Baumann C, Delezoide AL, Verloes A. Gérard-Blanluet M, et al. Among authors: baumann c. Fetal Pediatr Pathol. 2011;30(1):22-6. doi: 10.3109/15513815.2010.494698. Fetal Pediatr Pathol. 2011. PMID: 21204662

2

A new syndrome of congenital generalized osteosclerosis and bilateral polymicrogyria.

Titomanlio L, Baumann C, Bonyhay G, Huten Y, Oury JF, Vuillard E, Garel C, Terdjman P, Verloes A, Delezoide AL. Titomanlio L, et al. Among authors: baumann c. Am J Med Genet A. 2005 Sep 15;138(1):1-5. doi: 10.1002/ajmg.a.30914. Am J Med Genet A. 2005. PMID: 16097005

3

Unilateral agenesis of the abdominal wall musculature: An early muscle deficiency.

Gerard-Blanluet M, Port-Lis M, Baumann C, Perrin-Sabourin L, Ebrad P, Audry G, Delezoide AL, Verloes A. Gerard-Blanluet M, et al. Among authors: baumann c. Am J Med Genet A. 2010 Nov;152A(11):2870-4. doi: 10.1002/ajmg.a.33708. Am J Med Genet A. 2010. PMID: 20949627

4

Three patients with hallucal polydactyly and WAGR syndrome, including discordant expression of Wilms tumor in MZ twins.

Brémond-Gignac D, Gérard-Blanluet M, Copin H, Bitoun P, Baumann C, Crolla JA, Benzacken B, Verloes A. Brémond-Gignac D, et al. Among authors: baumann c. Am J Med Genet A. 2005 May 1;134(4):422-5. doi: 10.1002/ajmg.a.30646. Am J Med Genet A. 2005. PMID: 15779023

5

Gracile bones, periostal appositions, hypomineralization of the cranial vault, and mental retardation in brothers: milder variant of osteocraniostenosis or new syndrome?

Verloes A, Garel C, Robertson S, Le Merrer M, Baumann C. Verloes A, et al. Among authors: baumann c. Am J Med Genet A. 2005 Aug 30;137(2):199-203. doi: 10.1002/ajmg.a.30360. Am J Med Genet A. 2005. PMID: 16086393

6

A locus for sacral/anorectal malformations maps to 6q25.3 in a 0.3 Mb interval region.

Titomanlio L, Giurgea I, Baumann C, Elmaleh M, Sachs P, Chalard F, Aboura A, Verloes A. Titomanlio L, et al. Among authors: baumann c. Eur J Hum Genet. 2006 Aug;14(8):971-4. doi: 10.1038/sj.ejhg.5201635. Epub 2006 May 17. Eur J Hum Genet. 2006. PMID: 16724010

7

Abnormal abdominal situs: what and how should we look for?

Salomon LJ, Baumann C, Delezoide AL, Oury JF, Pariente D, Sebag G, Garel C. Salomon LJ, et al. Among authors: baumann c. Prenat Diagn. 2006 Mar;26(3):282-5. doi: 10.1002/pd.1401. Prenat Diagn. 2006. PMID: 16506280

8

Humero-radial synostosis, microcephaly, short corpus callosum, and abnormal genitalia in sibs.

Guilherme R, Baumann C, Garel C, Huten Y, Oury JF, Delezoide AL. Guilherme R, et al. Among authors: baumann c. Am J Med Genet A. 2008 Jul 15;146A(14):1775-80. doi: 10.1002/ajmg.a.32380. Am J Med Genet A. 2008. PMID: 18553517 Review.

9

Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome.

Bélien V, Gérard-Blanluet M, Serero S, Le Dû N, Baumann C, Jacquemont ML, Dupont C, Krabchi K, Drunat S, Elbez A, Janaud JC, Benzacken B, Verloes A, Tabet AC, Aboura A. Bélien V, et al. Among authors: baumann c. Am J Med Genet A. 2008 Jul 15;146A(14):1871-4. doi: 10.1002/ajmg.a.32392. Am J Med Genet A. 2008. PMID: 18553551

10

Prenatal diagnosis of trisomy 4p: a new locus for holoprosencephaly?

Karmous-Benailly H, Tabet AC, Thaly A, Dupuy O, Huten Y, Luton D, Baumann C, Delezoide AL. Karmous-Benailly H, et al. Among authors: baumann c. Prenat Diagn. 2005 Mar;25(3):193-7. doi: 10.1002/pd.1102. Prenat Diagn. 2005. PMID: 15791668

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