Stańczak H - Search Results

1

Familial four breakpoint complex chromosomal rearrangement as a cause of monosomy 9p22-->pter and trisomy 10p11.2-->pter and 11q21 analysed by dual and triple colour FISH.

Stankiewicz P, Kostyk E, Bocian E, Stańczak H, Parczewska J, Piatkowska E, Mazurczak T, Pietrzyk JJ. Stankiewicz P, et al. Among authors: stanczak h. J Med Genet. 1997 Aug;34(8):696-9. doi: 10.1136/jmg.34.8.696. J Med Genet. 1997. PMID: 9279768 Free PMC article.

2

Triple structural mosaicism of chromosome 18 in a child with MR/MCA syndrome and abnormal skin pigmentation.

Bocian E, Mazurczak T, Buława E, Stańczak H, Rowicka G. Bocian E, et al. Among authors: stanczak h. J Med Genet. 1993 Jul;30(7):614-5. doi: 10.1136/jmg.30.7.614. J Med Genet. 1993. PMID: 8411041 Free PMC article.

3

Paracentric inversion inv(18)(q21.1q23) in a woman with recurrent spontaneous abortions.

Bocian E, Mazurczak T, Stanczak H. Bocian E, et al. Among authors: stanczak h. Am J Med Genet. 1990 Apr;35(4):592-3. doi: 10.1002/ajmg.1320350432. Am J Med Genet. 1990. PMID: 2333893 No abstract available.

4

Frequency of Fra X syndrome among institutionalized mentally retarded males in Poland.

Mazurczak T, Bocian E, Milewski M, Obersztyn E, Stańczak H, Bal J, Szamotulska K, Karwacki MW. Mazurczak T, et al. Among authors: stanczak h. Am J Med Genet. 1996 Jul 12;64(1):184-6. doi: 10.1002/(SICI)1096-8628(19960712)64:1<184::AID-AJMG32>3.0.CO;2-H. Am J Med Genet. 1996. PMID: 8826472

5

[Partial trisomy of chromosome 13--diagnosis confirmed with the FISH in situ hybridization technique].

Obersztyn E, Stankiewicz P, Bocian E, Stańczak H, Mazurczak T. Obersztyn E, et al. Among authors: stanczak h. Pediatr Pol. 1996 Mar;71(3):247-52. Pediatr Pol. 1996. PMID: 8966097 Polish.

6

[Use of molecular cytogenetic techniques for establishing the origin of chromosome markers in patients with Turner phenotype].

Bocian E, Stańczak H, Wiśniewski A, Mazurczak T, Stankiewicz P. Bocian E, et al. Among authors: stanczak h. Pediatr Pol. 1996 Mar;71(3):203-9. Pediatr Pol. 1996. PMID: 8966091 Polish.

7

[Marker chromosomes as a product of familial translocation (11;22) identified with molecular cytogenetic methods].

Stankiewicz P, Korniszewski L, Bocian E, Stańczak H. Stankiewicz P, et al. Among authors: stanczak h. Pediatr Pol. 1996 Mar;71(3):241-5. Pediatr Pol. 1996. PMID: 8966096 Polish.

8

[Cytogenetic studies in clinical diagnosis --analysis of 1611 examination results].

Bocian E, Mazurczak T, Stańczak H. Bocian E, et al. Among authors: stanczak h. Przegl Lek. 1995;52(1):5-9. Przegl Lek. 1995. PMID: 7784612 Polish.

9

[Evaluation of karyotypes of married couples in cases of spontaneous abortion].

Brycz-Witkowska J, Mazurczak T, Stańczak H. Brycz-Witkowska J, et al. Among authors: stanczak h. Ginekol Pol. 1985 Mar;56(3):127-31. Ginekol Pol. 1985. PMID: 4054663 Polish. No abstract available.

10

[Prenatal diagnosis of chromosomal aberrations in the second trimester of pregnancy--analysis of problems and diagnostic difficulties].

Bocian E, Mazurczak T, Jakubów K, Sosnowska K, Stańczak H, Teterwak U. Bocian E, et al. Among authors: stanczak h. Ginekol Pol. 1989 Jul-Sep;60(7-9):373-9. Ginekol Pol. 1989. PMID: 2702196 Polish.

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