Odent S - Search Results

1

ATP7A mutation with occipital horns and distal motor neuropathy: A continuum.

Fradin M, Lavillaureix A, Jaillard S, Quelin C, Sauleau P, Minot MC, Menard D, Edan G, Ceballos I, Treguier C, Proisy M, Magdelaine C, Lia AS, Odent S, Pasquier L. Fradin M, et al. Among authors: odent s. Eur J Med Genet. 2020 Dec;63(12):104087. doi: 10.1016/j.ejmg.2020.104087. Epub 2020 Oct 31. Eur J Med Genet. 2020. PMID: 33137485

2

Triphalangeal thumb and split foot in the same family.

Le Marec B, Odent S, Treguier C. Le Marec B, et al. Among authors: odent s. Genet Couns. 1990;1(3-4):251-8. Genet Couns. 1990. PMID: 2098049

3

A case of Larsen syndrome with severe cervical malformations.

Le Marec B, Chapuis M, Tréguier C, Odent S, Bracq H. Le Marec B, et al. Among authors: odent s. Genet Couns. 1994;5(2):179-81. Genet Couns. 1994. PMID: 7917129

4

[Diffuse subcortical heterotopias of the gray matter].

Treguier C, Muh P, Le Berre C, Sorel L, Odent S, Dacher JN, Carsin M. Treguier C, et al. Among authors: odent s. Pediatrie. 1993;48(3):223-7. Pediatrie. 1993. PMID: 8393979 French.

5

Prenatal detection of a congenital pancreatic cyst and Beckwith-Wiedemann syndrome.

Fremond B, Poulain P, Odent S, Milon J, Treguier C, Babut JM. Fremond B, et al. Among authors: odent s. Prenat Diagn. 1997 Mar;17(3):276-80. Prenat Diagn. 1997. PMID: 9110373

6

Central nervous system malformations and early end-stage renal disease in oro-facio-digital syndrome type I: a review.

Odent S, Le Marec B, Toutain A, David A, Vigneron J, Tréguier C, Jouan H, Milon J, Fryns JP, Verloes A. Odent S, et al. Am J Med Genet. 1998 Feb 3;75(4):389-94. Am J Med Genet. 1998. PMID: 9482645 Review.

7

Gastric carcinoma in Sotos syndrome (cerebral gigantism).

Le Marec B, Pasquier L, Dugast C, Gosselin M, Odent S. Le Marec B, et al. Among authors: odent s. Ann Genet. 1999;42(2):113-6. Ann Genet. 1999. PMID: 10434127 Review.

8

A new mutation in the six-domain of SIX3 gene causes holoprosencephaly.

Pasquier L, Dubourg C, Blayau M, Lazaro L, Le Marec B, David V, Odent S. Pasquier L, et al. Among authors: odent s. Eur J Hum Genet. 2000 Oct;8(10):797-800. doi: 10.1038/sj.ejhg.5200540. Eur J Hum Genet. 2000. PMID: 11039582

9

Overgrowth and trisomy 15q26.1-qter including the IGF1 receptor gene: report of two families and review of the literature.

Faivre L, Gosset P, Cormier-Daire V, Odent S, Amiel J, Giurgea I, Nassogne MC, Pasquier L, Munnich A, Romana S, Prieur M, Vekemans M, De Blois MC, Turleau C. Faivre L, et al. Among authors: odent s. Eur J Hum Genet. 2002 Nov;10(11):699-706. doi: 10.1038/sj.ejhg.5200879. Eur J Hum Genet. 2002. PMID: 12404101

10

Molecular screening of the TGIF gene in holoprosencephaly: identification of two novel mutations.

Aguilella C, Dubourg C, Attia-Sobol J, Vigneron J, Blayau M, Pasquier L, Lazaro L, Odent S, David V. Aguilella C, et al. Among authors: odent s. Hum Genet. 2003 Feb;112(2):131-4. doi: 10.1007/s00439-002-0862-8. Epub 2002 Nov 21. Hum Genet. 2003. PMID: 12522553

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