Bartsch O - Search Results

1

Partial trisomy of 3q detected by chromosome painting in a case of juvenile chronic myelomonocytic leukemia.

Michalová K, Bartsch O, Starý J, Jelínek J, Wiegant J, Bubanská E. Michalová K, et al. Among authors: bartsch o. Cancer Genet Cytogenet. 1993 Nov;71(1):67-70. doi: 10.1016/0165-4608(93)90203-x. Cancer Genet Cytogenet. 1993. PMID: 8275454

2

Derivative (6)t(1;6)(q22;p21) revealed in bone marrow cells by FISH 9 months before diagnosis of acute T-lymphoblastic leukemia.

Michalová K, Lemez P, Bartsch O, Brĕzinová J, Zemanová Z, Jelínek J, Horák ID, Burke PJ. Michalová K, et al. Among authors: bartsch o. Cancer Genet Cytogenet. 1996 Feb;86(2):131-5. doi: 10.1016/0165-4608(95)00199-9. Cancer Genet Cytogenet. 1996. PMID: 8603339 Free article.

3

Clinical diagnosis of partial duplication 7q.

Bartsch O, Kalbe U, Ngo TK, Lettau R, Schwinger E. Bartsch O, et al. Am J Med Genet. 1990 Oct;37(2):254-7. doi: 10.1002/ajmg.1320370218. Am J Med Genet. 1990. PMID: 2248294

4

Boy with celiac disease, malformations, and ring chromosome 13 with deletion 13q32-->qter.

Talvik I, Ounap K, Bartsch O, Ilus T, Uibo O, Talvik T. Talvik I, et al. Among authors: bartsch o. Am J Med Genet. 2000 Aug 28;93(5):399-402. Am J Med Genet. 2000. PMID: 10951464

5

"Compensatory" uniparental disomy of chromosome 21 in two cases.

Bartsch O, Petersen MB, Stuhlmann I, Mau G, Frantzen M, Schwinger E, Antonarakis SE, Mikkelsen M. Bartsch O, et al. J Med Genet. 1994 Jul;31(7):534-40. doi: 10.1136/jmg.31.7.534. J Med Genet. 1994. PMID: 7966190 Free PMC article.

6

Trisomy of 8q22.3 approximately q23-qter following an unbalanced 1;8 translocation in a boy with multiple anomalies.

Ergun MA, Balci S, Konaç E, Kan D, Menevşe S, Bartsch O. Ergun MA, et al. Among authors: bartsch o. Turk J Pediatr. 2004 Oct-Dec;46(4):384-7. Turk J Pediatr. 2004. PMID: 15641279

7

Cytogenetic, FISH and DNA studies in 11 individuals from a family with two siblings with dup(21q) Down syndrome.

Bartsch O, König U, Petersen MB, Poulsen H, Mikkelsen M, Palau F, Prieto F, Schwinger E. Bartsch O, et al. Hum Genet. 1993 Sep;92(2):127-32. doi: 10.1007/BF00219679. Hum Genet. 1993. PMID: 8370577

8

Girl with combined cellular immunodeficiency, pancytopenia, malformations, deletion 11q23.3 --> qter, and trisomy 8q24.3 --> qter.

Ounap K, Bartsch O, Uibo O, Laidre P. Ounap K, et al. Among authors: bartsch o. Am J Med Genet. 2002 Apr 1;108(4):322-6. doi: 10.1002/ajmg.10284. Am J Med Genet. 2002. PMID: 11920839

9

A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region.

Bartsch O, Hinkel GK, Petersen MB, König U, Bugge M, Mikkelsen M, Avramopoulos D, Morris M, Antonarakis SE. Bartsch O, et al. Hum Genet. 1997 Oct;100(5-6):669-75. doi: 10.1007/s004390050571. Hum Genet. 1997. PMID: 9341890

10

Two novel deletions (array CGH findings) in pigment dispersion syndrome.

Mikelsaar R, Molder H, Bartsch O, Punab M. Mikelsaar R, et al. Among authors: bartsch o. Ophthalmic Genet. 2007 Dec;28(4):216-9. doi: 10.1080/13816810701635269. Ophthalmic Genet. 2007. PMID: 18161622

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