Palka G - Search Results

1

Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene.

Stuppia L, Gatta V, Mastroprimiano G, Pompetti F, Calabrese G, Guanciali Franchi P, Morizio E, Mingarelli R, Nicolai M, Tenaglia R, Improta L, Sforza V, Bisceglia S, Palka G. Stuppia L, et al. Among authors: palka g. J Med Genet. 1997 Nov;34(11):881-3. doi: 10.1136/jmg.34.11.881. J Med Genet. 1997. PMID: 9391878 Free PMC article.

2

Detection of minimal residual disease by polymerase chain reaction in patients with different hematologic diseases treated by bone marrow transplantation.

Stuppia L, Calabrese G, Guanciali Franchi P, Di Bartolomeo P, Antonucci A, Peila R, Torlontano G, Palka G. Stuppia L, et al. Among authors: palka g. Cancer Genet Cytogenet. 1993 Feb;65(2):88-92. doi: 10.1016/0165-4608(93)90212-5. Cancer Genet Cytogenet. 1993. PMID: 8453609

3

Duplication Xp22.2 and pseudoisodicentric Yq detected by FISH and PCR in a sterile male.

Palka G, Calabrese G, Mingarelli R, Guanciali Franchi P, Stuppia L, Morizio E, Peila R, Antonucci A. Palka G, et al. Clin Genet. 1995 Oct;48(4):213-6. doi: 10.1111/j.1399-0004.1995.tb04091.x. Clin Genet. 1995. PMID: 8591674

4

Molecular studies in three patients with isodicentric Y chromosome.

Stuppia L, Calabrese G, Franchi PG, Mingarelli R, Morizio E, Sabatino G, Palka G. Stuppia L, et al. Among authors: palka g. Hum Genet. 1996 Dec;98(6):691-5. doi: 10.1007/s004390050286. Hum Genet. 1996. PMID: 8931702

5

Microdeletions in interval 6 of the Y chromosome detected by STS-PCR in 6 of 33 patients with idiopathic oligo- or azoospermia.

Stuppia L, Mastroprimiano G, Calabrese G, Peila R, Tenaglia R, Palka G. Stuppia L, et al. Among authors: palka g. Cytogenet Cell Genet. 1996;72(2-3):155-8. doi: 10.1159/000134174. Cytogenet Cell Genet. 1996. PMID: 8978761

6

A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11.

Stuppia L, Gatta V, Calabrese G, Guanciali Franchi P, Morizio E, Bombieri C, Mingarelli R, Sforza V, Frajese G, Tenaglia R, Palka G. Stuppia L, et al. Among authors: palka g. Hum Genet. 1998 May;102(5):566-70. doi: 10.1007/s004390050741. Hum Genet. 1998. PMID: 9654206

7

Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane gene.

Calabrese G, Stuppia L, Morizio E, Guanciali Franchi P, Pompetti F, Mingarelli R, Marsilio T, Rocchi M, Gallenga PE, Palka G, Dallapiccola B. Calabrese G, et al. Among authors: palka g. Eur J Hum Genet. 1998 May-Jun;6(3):187-93. doi: 10.1038/sj.ejhg.5200173. Eur J Hum Genet. 1998. PMID: 9781021

8

Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male.

Stuppia L, Calabrese G, Borrelli P, Gatta V, Morizio E, Mingarelli R, Di Gilio MC, Crinò A, Giannotti A, Rappold GA, Palka G. Stuppia L, et al. Among authors: palka g. J Med Genet. 1999 Sep;36(9):711-3. J Med Genet. 1999. PMID: 10507731 Free PMC article.

9

FISH analysis in detecting 9p duplication (p22p24).

Guanciali Franchi P, Calabrese G, Morizio E, Modestini E, Stuppia L, Mingarelli R, Palka G. Guanciali Franchi P, et al. Among authors: palka g. Am J Med Genet. 2000 Jan 3;90(1):35-7. Am J Med Genet. 2000. PMID: 10602115

10

Characterization of a new TSPY gene family member in Yq (TSPYq1).

Ratti A, Stuppia L, Gatta V, Fogh I, Calabrese G, Pizzuti A, Palka G. Ratti A, et al. Among authors: palka g. Cytogenet Cell Genet. 2000;88(1-2):159-62. doi: 10.1159/000015510. Cytogenet Cell Genet. 2000. PMID: 10773691

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