Giuffrè L - Search Results

1

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: giuffre l. Am J Med Genet. 1995 Jan 30;55(3):315-8. doi: 10.1002/ajmg.1320550314. Am J Med Genet. 1995. PMID: 7726229

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: giuffre l. Am J Med Genet. 1990 Oct;37(2):244-9. doi: 10.1002/ajmg.1320370216. Am J Med Genet. 1990. PMID: 2147361

3

The fragile X in Sicily: an epidemiological survey.

Neri G, Sanfilippo S, Pavone L, Mollica F, Barberi I, Giuffrè L, Romano C, Mattina T, Cammarata M, Ragusa MG, et al. Neri G, et al. Among authors: giuffre l. Am J Med Genet. 1988 May-Jun;30(1-2):665-72. doi: 10.1002/ajmg.1320300167. Am J Med Genet. 1988. PMID: 3177477

4

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. Klin Padiatr. 1988 Jan-Feb;200(1):10-4. doi: 10.1055/s-2008-1033677. Klin Padiatr. 1988. PMID: 3367608

5

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: giuffre l. Am J Med Genet. 1992 Dec 1;44(6):813-5. doi: 10.1002/ajmg.1320440619. Am J Med Genet. 1992. PMID: 1481853

6

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: giuffre l. Am J Med Genet Suppl. 1990;7:66-70. doi: 10.1002/ajmg.1320370712. Am J Med Genet Suppl. 1990. PMID: 2149977

7

New syndrome: autosomal dominant microcephaly and radio-ulnar synostosis.

Giuffrè L, Corsello G, Giuffrè M, Piccione M, Albanese A. Giuffrè L, et al. Among authors: giuffre m. Am J Med Genet. 1994 Jul 1;51(3):266-9. doi: 10.1002/ajmg.1320510319. Am J Med Genet. 1994. PMID: 8074157

8

[Ring chromosome 4 in twins].

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

9

Genetic factors of recurrent abortions.

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

10

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

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

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