Ventruto V - Search Results

1

[Severe mental retardation and slight dysmorphism in a child with a bisatellite extrachromosome: inversion duplication (15)?].

Rinaldi MM, Militerni R, Pascotto A, Scarano G, Renda S, Cavaliere ML, Santulli B, Esposito M, Ventruto V. Rinaldi MM, et al. Among authors: ventruto v. Pediatr Med Chir. 1982 Sep-Oct;4(5):559-61. Pediatr Med Chir. 1982. PMID: 6927358 Italian.

2

[Aarskog's syndrome (facial-digital-genital syndrome). Study of a family (author's transl)].

Scarano G, Rinaldi MM, Cavaliere ML, Esposito M, Sicolo A, Santulli B, Stabile M, Fasano R, Ventruto V. Scarano G, et al. Among authors: ventruto v. Pediatr Med Chir. 1981 Jul-Aug;3(4):323-5. Pediatr Med Chir. 1981. PMID: 7343926 Italian.

3

Multiple skeletal familial abnormalities associated with balanced reciprocal translocation 2;8(q32;p13).

Ventruto V, Pisciotta R, Renda S, Festa B, Rinaldi MM, Stabile M, Cavaliere ML, Esposito M. Ventruto V, et al. Am J Med Genet. 1983 Dec;16(4):589-94. doi: 10.1002/ajmg.1320160416. Am J Med Genet. 1983. PMID: 6660251

4

[XXXXY syndrome: clinical-radiological findings in one patient (author's transl)].

Ventruto V, Pisciotta R, Celona A, Cavaliere ML, Pagano L, Stabile M, Fioretti G, Togo F. Ventruto V, et al. Radiol Med. 1981 Mar;67(3):147-51. Radiol Med. 1981. PMID: 7268086 Italian.

5

Clinical features of monosomy 10qter.

Zatterale A, Pagano L, Fioretti G, Caniglia M, Festa B, Renda S, Rinaldi MM, Ventruto V. Zatterale A, et al. Among authors: ventruto v. Ann Genet. 1983;26(2):106-8. Ann Genet. 1983. PMID: 6604483

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. 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. Pathologica. 1983;75 Suppl:258-61. Pathologica. 1983. PMID: 6680428 Italian. No abstract available.

8

[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: ventruto v. Minerva Pediatr. 1980 Jun 30;32(12):807-14. Minerva Pediatr. 1980. PMID: 7464734 Italian. No abstract available.

9

[Poland-Moebius syndrome. Description of a new case].

Scarano G, Sacco R, Lonardo F, Alfano A, Ventruto V. Scarano G, et al. Among authors: ventruto v. Pediatr Med Chir. 1986 Jan-Feb;8(1):111-2. Pediatr Med Chir. 1986. PMID: 3014448 Italian.

10

t(21q21q)/r[t(21q21q)] mosaic in two unrelated patients with mild stigmata of Down's syndrome.

Dallapiccola B, Bianco I, Brinchi V, Santulli B, Scarano G, Sicolo A, Stabile M, Ventruto V. Dallapiccola B, et al. Among authors: ventruto v. Ann Genet. 1982;25(1):56-8. Ann Genet. 1982. PMID: 6211124

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