Piussan C - Search Results

1

Collaborative study of mosaic tetrasomy 12p or Pallister-Killian syndrome (nineteen fetuses or children).

Mathieu M, Piussan C, Thepot F, Gouget A, Lacombe D, Pedespan JM, Serville F, Fontan D, Ruffie M, Nivelon-Chevallier A, Amblard F, Chauveau P, Moirot H, Chabrolle JP, Croquette MF, Teyssier M, Plauchu H, Pelissier MC, Gilgenkrantz S, Turc-Carel C, Turleau C, Prieur M, Le Merrer M, Gonzales M, Journel H, et al. Mathieu M, et al. Among authors: piussan c. Ann Genet. 1997;40(1):45-54. Ann Genet. 1997. PMID: 9150850

2

The KBG syndrome: an additional sporadic case.

Mathieu M, Helou M, Morin G, Dolhem P, Devauchelle B, Piussan C. Mathieu M, et al. Among authors: piussan c. Genet Couns. 2000;11(1):33-5. Genet Couns. 2000. PMID: 10756425

3

A familial syndrome with micrognathia, cleft palate, short neck and stature, vertebral anomalies and mental retardation.

Mathieu M, De Broca A, Bony H, Piussan C. Mathieu M, et al. Among authors: piussan c. Genet Couns. 1993;4(4):299-303. Genet Couns. 1993. PMID: 8110419

4

Fragile X mutation and FG syndrome-like phenotype.

Piussan C, Mathieu M, Berquin P, Fryns JP. Piussan C, et al. Am J Med Genet. 1996 Aug 9;64(2):395-8. doi: 10.1002/(SICI)1096-8628(19960809)64:2<395::AID-AJMG32>3.0.CO;2-8. Am J Med Genet. 1996. PMID: 8844090

5

[Dubowitz syndrome. A diagnosis not to be missed].

Mathieu M, Berquin P, Epelbaum S, Lenaerts C, Piussan C. Mathieu M, et al. Among authors: piussan c. Arch Fr Pediatr. 1991 Dec;48(10):715-8. Arch Fr Pediatr. 1991. PMID: 1793348 French.

6

[An example of detection of heterozygotes and antenatal diagnosis in four families with anhidrotic ectodermal dysplasia].

Szpiro-Tapia S, Kaplan J, Pelet A, Guilloud-Bataille M, Heuertz S, Nivelon-Chevallier A, Mathieu M, Piussan C, Journel H, Dodinval P, et al. Szpiro-Tapia S, et al. Among authors: piussan c. Ann Pediatr (Paris). 1990 Jan;37(1):13-9. Ann Pediatr (Paris). 1990. PMID: 2316957 French.

7

The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21).

Saugier-Veber P, Abadie V, Moncla A, Mathieu M, Piussan C, Turleau C, Mattei JF, Munnich A, Lyonnet S. Saugier-Veber P, et al. Among authors: piussan c. Am J Hum Genet. 1993 Jun;52(6):1040-5. Am J Hum Genet. 1993. PMID: 8503439 Free PMC article.

8

Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2.

Biancalana V, Briard ML, David A, Gilgenkrantz S, Kaplan J, Mathieu M, Piussan C, Poncin J, Schinzel A, Oudet C, et al. Biancalana V, et al. Among authors: piussan c. Am J Hum Genet. 1992 May;50(5):981-7. Am J Hum Genet. 1992. PMID: 1349200 Free PMC article.

9

[Teratogenic risk during treatment of Wilson disease].

Piussan C, Mathieu M. Piussan C, et al. J Genet Hum. 1985 Sep;33(3-4):357-62. J Genet Hum. 1985. PMID: 4056754 French.

10

[Regular dominance of thumb ankylosis with mental retardation transmitted over 3 generations].

Piussan C, Lenaerts C, Mathieu M, Boudailliez B. Piussan C, et al. J Genet Hum. 1983 Jun;31(2):107-14. J Genet Hum. 1983. PMID: 6631421 French.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

118 results

Search Page

Filters