Bortotto L[au] - Search Results

Year	Number of Results
1979	1
1982	1
1984	2
1986	1
1990	1
1991	1
1992	1
1998	1
2011	1
2024	0

1

Chromosome imbalance, normal phenotype, and imprinting.

Bortotto L, Piovan E, Furlan R, Rivera H, Zuffardi O. Bortotto L, et al. J Med Genet. 1990 Sep;27(9):582-7. doi: 10.1136/jmg.27.9.582. J Med Genet. 1990. PMID: 2231652 Free PMC article. Review.

2

Fetal gender ratio in recurrent miscarriages.

Del Fabro A, Driul L, Anis O, Londero AP, Bertozzi S, Bortotto L, Marchesoni D. Del Fabro A, et al. Among authors: bortotto l. Int J Womens Health. 2011;3:213-7. doi: 10.2147/IJWH.S20557. Epub 2011 Jul 20. Int J Womens Health. 2011. PMID: 21845066 Free PMC article.

3

Epidemiology of Friedreich's ataxia in the province of Reggio Emilia.

Lucci B, Bortotto L, Motti L, Guidetti D, Zucco R, Marchini C. Lucci B, et al. Among authors: bortotto l. Riv Neurobiol. 1984 Jan-Mar;30(1):5-10. Riv Neurobiol. 1984. PMID: 6544467 No abstract available.

4

Apparent CHARGE association and chromosome anomaly: chance or contiguous gene syndrome.

Clementi M, Tenconi R, Turolla L, Silvan C, Bortotto L, Artifoni L. Clementi M, et al. Among authors: bortotto l. Am J Med Genet. 1991 Nov 1;41(2):246-50. doi: 10.1002/ajmg.1320410223. Am J Med Genet. 1991. PMID: 1785643

5

Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndrome.

Tupler R, Bortotto L, Bühler EM, Alkan M, Malik NJ, Bösch-Al Jadooa N, Memo L, Maraschio P. Tupler R, et al. Among authors: bortotto l. J Med Genet. 1992 Jan;29(1):53-5. doi: 10.1136/jmg.29.1.53. J Med Genet. 1992. PMID: 1552546 Free PMC article.

6

Agenesis of the corpus callosum with Probst bundles owing to haploinsufficiency for a gene in an 8 cM region of 6q25.

Pirola B, Bortotto L, Giglio S, Piovan E, Janes A, Guerrini R, Zuffardi O. Pirola B, et al. Among authors: bortotto l. J Med Genet. 1998 Dec;35(12):1031-3. doi: 10.1136/jmg.35.12.1031. J Med Genet. 1998. PMID: 9863602 Free PMC article.

7

[Use of some methods of banding for the study of human polymorphisms].

Artifoni L, Bortotto L, Goppion G, Baccichetti C. Artifoni L, et al. Among authors: bortotto l. Pathologica. 1979 May-Jun;71(1013):397-9. Pathologica. 1979. PMID: 548890 Italian. No abstract available.

8

Study on segregation of the inversion of chromosome 4 (p15.2q11) in two unrelated families.

Baccichetti C, Tenconi R, Caufin D, Bortotto L. Baccichetti C, et al. Among authors: bortotto l. Hum Genet. 1982;62(2):117-20. doi: 10.1007/BF00282297. Hum Genet. 1982. PMID: 7160843 No abstract available.

9

Trisomy 9p due to unusual maternal translocation (3;9).

Calzolari E, Contiero MR, Aiello V, Bortotto L. Calzolari E, et al. Among authors: bortotto l. J Med Genet. 1984 Aug;21(4):320. doi: 10.1136/jmg.21.4.320. J Med Genet. 1984. PMID: 6492100 Free PMC article. No abstract available.

10

[Acute leukemia secondary to idiopathic myelofibrosis with homozygote pseudo-Pelger anomaly and complex chromosomal changes].

Tosato F, Fossaluzza V, Bortotto L, Bartolomei P. Tosato F, et al. Among authors: bortotto l. Minerva Med. 1986 May 31;77(22-23):1023-6. Minerva Med. 1986. PMID: 3459966 Italian.

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