Baumann C - Search Results

1

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

2

Severely delayed epiphyseal ossification dysplasia with normal stature.

Baumann C, Garel C, Vuillemain L, Hassan M, Verloes A. Baumann C, et al. Am J Med Genet A. 2003 Aug 1;120A(4):553-6. doi: 10.1002/ajmg.a.20046. Am J Med Genet A. 2003. PMID: 12884438

3

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

4

Michels syndrome, Carnevale syndrome, OSA syndrome, and Malpuech syndrome: variable expression of a single disorder (3MC syndrome)?

Titomanlio L, Bennaceur S, Bremond-Gignac D, Baumann C, Dupuy O, Verloes A. Titomanlio L, et al. Among authors: baumann c. Am J Med Genet A. 2005 Sep 1;137A(3):332-5. doi: 10.1002/ajmg.a.30878. Am J Med Genet A. 2005. PMID: 16096999 Review.

5

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.

6

Spondylometaphyseal dysplasia, east-African type: a new form of early, severe SMD with rounded vertebrae.

Verloes A, Lepage P, Baumann C, Maroteaux P, Merrer ML. Verloes A, et al. Among authors: baumann c. Am J Med Genet. 2002 Dec 15;113(4):362-6. doi: 10.1002/ajmg.b.10738. Am J Med Genet. 2002. PMID: 12457408

7

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

8

Neuropathic visceral dysmotility, brain cysts and calcifications, facial dysmorphism and developmental delay in two sibs. A new syndrome?

Hadchouel A, Bellaiche M, Baumann C, Darnaud G, El Ghoneimi A, Ferkdadji L, Elmaleh M, Verloes A. Hadchouel A, et al. Among authors: baumann c. Eur J Med Genet. 2005 Oct-Dec;48(4):367-76. doi: 10.1016/j.ejmg.2005.05.006. Epub 2005 Jun 16. Eur J Med Genet. 2005. PMID: 16378921

9

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

10

Blepharophimosis-mental retardation (BMR) syndromes: A proposed clinical classification of the so-called Ohdo syndrome, and delineation of two new BMR syndromes, one X-linked and one autosomal recessive.

Verloes A, Bremond-Gignac D, Isidor B, David A, Baumann C, Leroy MA, Stevens R, Gillerot Y, Héron D, Héron B, Benzacken B, Lacombe D, Brunner H, Bitoun P. Verloes A, et al. Among authors: baumann c. Am J Med Genet A. 2006 Jun 15;140(12):1285-96. doi: 10.1002/ajmg.a.31270. Am J Med Genet A. 2006. PMID: 16700052

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