Caiulo A - Search Results

1

Deletion of the distal short arm of the X chromosome (Xp) in a patient with short stature, chondrodysplasia punctata, and X-linked ichthyosis due to steroid sulfatase deficiency.

Ballabio A, Zollo M, Carrozzo R, Caiulo A, Zuffardi O, Cascioli CF, Viggiano D, Strisciuglio P. Ballabio A, et al. Among authors: caiulo a. Am J Med Genet. 1991 Nov 1;41(2):184-7. doi: 10.1002/ajmg.1320410210. Am J Med Genet. 1991. PMID: 1785631

2

Evidence for an ancestral alphoid domain on the long arm of human chromosome 2.

Avarello R, Pedicini A, Caiulo A, Zuffardi O, Fraccaro M. Avarello R, et al. Among authors: caiulo a. Hum Genet. 1992 May;89(2):247-9. doi: 10.1007/BF00217134. Hum Genet. 1992. PMID: 1587535

3

Deletion of specific sequences or modification of centromeric chromatin are responsible for Y chromosome centromere inactivation.

Maraschio P, Zuffardi O, Caiulo A, Dainotti E, Piantanida M, Rivera H, Tupler R. Maraschio P, et al. Among authors: caiulo a. Hum Genet. 1990 Oct;85(5):491-4. doi: 10.1007/BF00194222. Hum Genet. 1990. PMID: 2227932

4

[An update on gonadal differentiation].

Zuffardi O, Caiulo A. Zuffardi O, et al. Among authors: caiulo a. Pediatr Med Chir. 1989 Sep-Oct;11(5):481-4. Pediatr Med Chir. 1989. PMID: 2517143 Review. Italian.

5

Regional assignment of the loci for adenylate kinase to 9q32 and for alpha 1-acid glycoprotein to 9q31-q32. A locus for Goltz syndrome in region 9q32-qter?

Zuffardi O, Caiulo A, Maraschio P, Tupler R, Bianchi E, Amisano P, Beluffi G, Moratti R, Liguri G. Zuffardi O, et al. Among authors: caiulo a. Hum Genet. 1989 Apr;82(1):17-9. doi: 10.1007/BF00288264. Hum Genet. 1989. PMID: 2541064

6

Alternate centromere inactivation in a pseudodicentric (15;20)(pter;pter) associated with a progressive neurological disorder.

Rivera H, Zuffardi O, Maraschio P, Caiulo A, Anichini C, Scarinci R, Vivarelli R. Rivera H, et al. Among authors: caiulo a. J Med Genet. 1989 Oct;26(10):626-30. doi: 10.1136/jmg.26.10.626. J Med Genet. 1989. PMID: 2685311 Free PMC article.

7

Mapping the gene encoding the human erythroid transcriptional factor NFE1-GF1 to Xp11.23.

Caiulo A, Nicolis S, Bianchi P, Zuffardi O, Bardoni B, Maraschio P, Ottolenghi S, Camerino G, Giglioni B. Caiulo A, et al. Hum Genet. 1991 Feb;86(4):388-90. doi: 10.1007/BF00201840. Hum Genet. 1991. PMID: 1999341

8

Cytogenetic and molecular analysis of an unbalanced translocation (X;7) (q28;p15) in a dysmorphic girl.

Caiulo A, Bardoni B, Camerino G, Guioli S, Minelli A, Piantanida M, Crosato F, Dalla Fior T, Maraschio P. Caiulo A, et al. Hum Genet. 1989 Dec;84(1):51-4. doi: 10.1007/BF00210670. Hum Genet. 1989. PMID: 2558067

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