Stoll C - Search Results

1

Epidemiology of Down syndrome in 118,265 consecutive births.

Stoll C, Alembik Y, Dott B, Roth MP. Stoll C, et al. Am J Med Genet Suppl. 1990;7:79-83. doi: 10.1002/ajmg.1320370715. Am J Med Genet Suppl. 1990. PMID: 2149980

2

An epidemiologic study of environmental and genetic factors in congenital hydrocephalus.

Stoll C, Alembik Y, Dott B, Roth MP. Stoll C, et al. Eur J Epidemiol. 1992 Nov;8(6):797-803. doi: 10.1007/BF00145322. Eur J Epidemiol. 1992. PMID: 1294384

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. Am J Med Genet. 1992 Feb 15;42(4):480-6. doi: 10.1002/ajmg.1320420413. Am J Med Genet. 1992. PMID: 1376967

4

Epidemiology of congenital eye malformations in 131,760 consecutive births.

Stoll C, Alembik Y, Dott B, Roth MP. Stoll C, et al. Ophthalmic Paediatr Genet. 1992 Sep;13(3):179-86. doi: 10.3109/13816819209046487. Ophthalmic Paediatr Genet. 1992. PMID: 1484696

5

[Fragile X chromosome in autism and psychotic disorders in children].

Bursztejn C, Alembik Y, Stoll C, Poupier G, Feller L, Hamon J, Tribout JL, Gardone MC, Danion-Grilliat A. Bursztejn C, et al. Among authors: stoll c. Arch Fr Pediatr. 1992 Feb;49(2):99-103. Arch Fr Pediatr. 1992. PMID: 1580745 Review. French.

6

Arthrogryposis, ectodermal dysplasia and other anomalies in two sisters.

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

7

Evaluation of prenatal diagnosis by a registry of congenital anomalies.

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

8

Risk factors in limb reduction defects.

Stoll C, Alembik Y, Dott B, Roth MP. Stoll C, et al. Paediatr Perinat Epidemiol. 1992 Jul;6(3):323-38. doi: 10.1111/j.1365-3016.1992.tb00773.x. Paediatr Perinat Epidemiol. 1992. PMID: 1635883

9

[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. Arch Fr Pediatr. 1991 Oct;48(8):549-54. Arch Fr Pediatr. 1991. PMID: 1768194 Review. French.

10

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. Genet Couns. 1991;2(4):211-5. Genet Couns. 1991. PMID: 1799418

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