Cammarata M - Search Results

1

Cammarata M, Corsello G, Marino M, Morabito M, Pecoraro MR, Piccione M, Giuffrè L. Cammarata M, et al. Acta Eur Fertil. 1989 Nov-Dec;20(6):367-70. Acta Eur Fertil. 1989. PMID: 2488982

2

Holoprosencephaly: examples of clinical variability and etiologic heterogeneity.

Corsello G, Buttitta P, Cammarata M, Lo Presti A, Maresi E, Zumpani L, Giuffrè L. Corsello G, et al. Among authors: cammarata m. Am J Med Genet. 1990 Oct;37(2):244-9. doi: 10.1002/ajmg.1320370216. Am J Med Genet. 1990. PMID: 2147361

3

Two new cases of thrombocytopenia absent radius (TAR) syndrome: clinical, genetic and nosologic features.

Giuffrè L, Cammarata M, Corsello G, Vitaliti SM. Giuffrè L, et al. Among authors: cammarata m. Klin Padiatr. 1988 Jan-Feb;200(1):10-4. doi: 10.1055/s-2008-1033677. Klin Padiatr. 1988. PMID: 3367608

4

[Role of diagnostic imaging in Rubinstein-Taybi syndrome. Personal experience with 8 cases].

Albanese A, Giuffrè L, Carcione A, Corsello G, Benenati A, Cammarata M, Albano S, Piccione M, Rubino FP, Reina C, et al. Albanese A, et al. Among authors: cammarata m. Radiol Med. 1991 Mar;81(3):253-61. Radiol Med. 1991. PMID: 2014329 Italian.

5

Growth charts of Down syndrome in Sicily: evaluation of 382 children 0-14 years of age.

Piro E, Pennino C, Cammarata M, Corsello G, Grenci A, Lo Giudice C, Morabito M, Piccione M, Giuffrè L. Piro E, et al. Among authors: cammarata m. Am J Med Genet Suppl. 1990;7:66-70. doi: 10.1002/ajmg.1320370712. Am J Med Genet Suppl. 1990. PMID: 2149977

6

[Ring chromosome 4 in twins].

Giuffrè L, Cammarata M, Corsello G, Benigno V, Graziano L, Roccella F, Balsamo V. Giuffrè L, et al. Among authors: cammarata m. Pediatr Med Chir. 1987 May-Jun;9(3):349-50. Pediatr Med Chir. 1987. PMID: 3671134 Italian.

7

VATER/VACTERL association: clinical variability and expanding phenotype including laryngeal stenosis.

Corsello G, Maresi E, Corrao AM, Dimita U, Lo Cascio M, Cammarata M, Giuffrè L. Corsello G, et al. Among authors: cammarata m. Am J Med Genet. 1992 Dec 1;44(6):813-5. doi: 10.1002/ajmg.1320440619. Am J Med Genet. 1992. PMID: 1481853

8

[Male pseudohermaphroditism related to 17-alpha hydroxylase deficiency].

Liotta A, Cammarata M, Corsello G, Ferrara D, Giuffrè L. Liotta A, et al. Among authors: cammarata m. Pediatr Med Chir. 1987 May-Jun;9(3):309-10. Pediatr Med Chir. 1987. PMID: 2823235 Italian.

9

Ulnar ray defect in an infant with a 6q21;7q31.2 translocation: further evidence for the existence of a limb defect gene in 6q21.

Gurrieri F, Cammarata M, Avarello RM, Genuardi M, Pomponi MG, Neri G, Giuffrè L. Gurrieri F, et al. Among authors: cammarata m. Am J Med Genet. 1995 Jan 30;55(3):315-8. doi: 10.1002/ajmg.1320550314. Am J Med Genet. 1995. PMID: 7726229

10

[Down's syndrome with unusual karyotype: tandem duplication of chromosome 21].

Giuffrè L, Cammarata M, Corsello G, Pecoraro MR, Piccione M, Vitaliti SM. Giuffrè L, et al. Among authors: cammarata m. Minerva Pediatr. 1988 May;40(5):287-90. Minerva Pediatr. 1988. PMID: 2971868 Italian. No abstract available.

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

274 results

Search Page

Filters