Finck S - Search Results

1

[Congenital malformations in a series of 131,760 consecutive births during 10 years].

Stoll C, Dott B, Alembik Y, Roth MP, Finck S. Stoll C, et al. Among authors: finck s. Arch Fr Pediatr. 1991 Oct;48(8):549-54. Arch Fr Pediatr. 1991. PMID: 1768194 Review. French.

2

Evaluation of prenatal diagnosis by a registry of congenital anomalies.

Stoll C, Alembik Y, Dott B, Roth MP, Finck S. Stoll C, et al. Among authors: finck s. Prenat Diagn. 1992 Apr;12(4):263-70. doi: 10.1002/pd.1970120405. Prenat Diagn. 1992. PMID: 1614983

3

Ventricular extrasystoles with syncopal episodes, perodactyly, and Robin in sequence in three generations: a new inherited MCA syndrome?

Stoll C, Kieny JR, Dott B, Alembik Y, Finck S. Stoll C, et al. Among authors: finck s. Am J Med Genet. 1992 Feb 15;42(4):480-6. doi: 10.1002/ajmg.1320420413. Am J Med Genet. 1992. PMID: 1376967

4

Arthrogryposis, ectodermal dysplasia and other anomalies in two sisters.

Stoll C, Alembik Y, Finck S, Janser B. Stoll C, et al. Among authors: finck s. Genet Couns. 1992;3(1):35-9. Genet Couns. 1992. PMID: 1590979

5

Tau syndrome (thrombocytopenia and absent ulnar) with mental retardation and facial dysmorphy.

Stoll C, Finck S, Janser B, Printz M, Lutz P. Stoll C, et al. Among authors: finck s. Genet Couns. 1992;3(1):41-7. Genet Couns. 1992. PMID: 1590980

6

Are some multiple congenital anomalies with mental retardation (MCA/MR) the clinical expression of rare autosomal fragile sites?

Stoll C, Bolender C, Geraudel A, Finck S, Alembik Y, Dott B. Stoll C, et al. Among authors: finck s. Genet Couns. 1991;2(4):211-5. Genet Couns. 1991. PMID: 1799418

7

[Anomalies of thyroid function in children with Down syndrome].

Toledo C, Alembik Y, Dott B, Finck S, Stoll C. Toledo C, et al. Among authors: finck s. Arch Pediatr. 1997 Feb;4(2):116-20. doi: 10.1016/s0929-693x(97)86151-9. Arch Pediatr. 1997. PMID: 9097820 French.

8

[Anomalies in thyroid function in children with trisomy 21].

Stoll C, Alembik Y, Dott B, Finck S. Stoll C, et al. Among authors: finck s. J Genet Hum. 1989 Dec;37(4-5):389-93. J Genet Hum. 1989. PMID: 2534560 French.

9

Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in males.

Biancalana V, Taine L, Bouix JC, Finck S, Chauvin A, De Verneuil H, Knight SJ, Stoll C, Lacombe D, Mandel JL. Biancalana V, et al. Among authors: finck s. Am J Hum Genet. 1996 Oct;59(4):847-54. Am J Hum Genet. 1996. PMID: 8808600 Free PMC article.

10

Landau-Kleffner syndrome: a pharmacologic study of five cases.

Marescaux C, Hirsch E, Finck S, Maquet P, Schlumberger E, Sellal F, Metz-Lutz MN, Alembik Y, Salmon E, Franck G. Marescaux C, et al. Among authors: finck s. Epilepsia. 1990 Nov-Dec;31(6):768-77. doi: 10.1111/j.1528-1157.1990.tb05518.x. Epilepsia. 1990. PMID: 1700953

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

45 results

Search Page

Filters