Rinaldi A - Search Results

1

A case of Edward's syndrome with pseudodicentric isochromosome 18: 46,XY,i dic(18) (p11::p11).

Fioretti G, Stabile M, Pagano L, Rinaldi A, Rolando D, Trapassi C, de Tollis G, Ventruto V. Fioretti G, et al. Among authors: rinaldi a. Ann Genet. 1982;25(2):116-8. Ann Genet. 1982. PMID: 6984627 No abstract available.

2

Hereditary 3;6 translocation : three cases of multiple malformations with partial trisomy 6p21 leads to pter.

Pagano L, Fioretti G, Vetrella M, Risolo E, Casullo C, Celona A, Renda S, Rinaldi A, Ventruto V. Pagano L, et al. Among authors: rinaldi a. Ann Genet. 1980;23(3):173-5. Ann Genet. 1980. PMID: 6968535

3

[Partial trisomy 10q24 leads to 10qter due to familial translocation (9;10) (p24;q24) recurring in 3 generations].

Stabile M, Scarano G, Rinaldi A, Fioretti G, Pagano L, Tancredi F, Della Pietra D, Renda S, Festa B, Ventruto V. Stabile M, et al. Among authors: rinaldi a. Minerva Pediatr. 1983 May 31;35(10):515-9. Minerva Pediatr. 1983. PMID: 6877198 Italian. No abstract available.

4

[Report of a case of partial trisomy 22:47,XX, + 22(p ter - q 12)].

Renda S, Bandieramonte Z, Pagano L, Rinaldi A, Fioretti G, Iozzino G, Stabile M, Cautiero O, Ventruto V. Renda S, et al. Among authors: rinaldi a. Pediatria (Napoli). 1980 Mar 31;88(1):91-7. Pediatria (Napoli). 1980. PMID: 7290814 Italian. No abstract available.

5

[Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation].

Fioretti G, Pagano L, Renda S, Festa B, Rinaldi A, Celona A, Casullo C, Stabile M, Cavaliere ML, Ventruto V. Fioretti G, et al. Among authors: rinaldi a. Minerva Pediatr. 1980 Jun 30;32(12):807-14. Minerva Pediatr. 1980. PMID: 7464734 Italian. No abstract available.

6

Ring (13),t(2;6) associated with familial fragile (16).

Ventruto V, Rinaldi A, Renda S, Stabile M, Rinaldi MM, Cavaliere ML, Conte N, Aveta V. Ventruto V, et al. Among authors: rinaldi a, rinaldi mm. J Med Genet. 1984 Jun;21(3):233. doi: 10.1136/jmg.21.3.233. J Med Genet. 1984. PMID: 6748026 Free PMC article. No abstract available.

7

[Phenotype anomalies in subjects with balanced chromosome translocation. Presentation of 4 cases].

Ventruto V, Festa B, Renda S, Stabile M, Rinaldi A, Rinaldi MM, Cavaliere ML, Lonardo F, Garofalo S. Ventruto V, et al. Among authors: rinaldi a, rinaldi mm. Pathologica. 1983;75 Suppl:258-61. Pathologica. 1983. PMID: 6680428 Italian. No abstract available.

8

Fragile-X mutation and Klinefelter syndrome: a reappraisal.

Filippi G, Pecile V, Rinaldi A, Siniscalco M. Filippi G, et al. Among authors: rinaldi a. Am J Med Genet. 1988 May-Jun;30(1-2):99-107. doi: 10.1002/ajmg.1320300108. Am J Med Genet. 1988. PMID: 3177482

9

Brief report: linkage between G6PD and fragile-X syndrome.

Filippi G, Rinaldi A, Archidiacono N, Rocchi M, Balazs I, Siniscalco M. Filippi G, et al. Among authors: rinaldi a. Am J Med Genet. 1983 May;15(1):113-9. doi: 10.1002/ajmg.1320150115. Am J Med Genet. 1983. PMID: 6602550

10

X-mapping in man: evidence against measurable linkage between anhidrotic ectodermal dysplasia and G6PD deficiency.

Filippi G, Rinaldi A, Crisponi G, Daniels GL, Siniscalco M. Filippi G, et al. Among authors: rinaldi a. J Med Genet. 1979 Jun;16(3):223-4. doi: 10.1136/jmg.16.3.223. J Med Genet. 1979. PMID: 469901 Free PMC article.

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