Bocian E - Search Results

1

[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: bocian e. Pediatr Pol. 1996 Mar;71(3):247-52. Pediatr Pol. 1996. PMID: 8966097 Polish.

2

[Cytogenetic-molecular analysis of balanced chromosomal rearrangements in nine patients with intellectual disability, dysmorphic features and congenital abnormalities].

Borg K, Bocian E, Stankiewicz P, Obersztyn E, Kruczek A, Nowakowska B, Ilnicka A, Mazurczak T. Borg K, et al. Among authors: bocian e. Med Wieku Rozwoj. 2006 Jan-Mar;10(1 Pt 2):227-46. Med Wieku Rozwoj. 2006. PMID: 17028391 Polish.

3

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

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

4

[Reliability of cytogenetic and clinical diagnostic studies. Results of analyzing 1621 pre- and postnatal studies].

Bocian E, Jakubów K, Stańczak H, Lewicka D, Mazurczak T. Bocian E, et al. Pediatr Pol. 1995 Oct;70(10):803-8. Pediatr Pol. 1995. PMID: 8649926 Polish.

5

[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. Pediatr Pol. 1996 Mar;71(3):203-9. Pediatr Pol. 1996. PMID: 8966091 Polish.

6

[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: bocian e. Pediatr Pol. 1996 Mar;71(3):241-5. Pediatr Pol. 1996. PMID: 8966096 Polish.

7

[Results of 1043 prenatal cytogenetic studies: retrospective study in the context of applicability of interphase FISH in prenatal diagnosis]].

Bocian E, Jakubów-Durska K, Mazurczak T. Bocian E, et al. Ginekol Pol. 2001 Jun;72(6):449-55. Ginekol Pol. 2001. PMID: 11526742 Polish.

8

[Case of subtelomeric aberration as a cause of familial intellectual disability with congenital defects and dysmorphic features--problems of diagnosis and genetic counseling].

Obersztyn E, Mazurczak T, Helias-Rodzewicz Z, Bocian E, Kutkowska-Kazmierczak A. Obersztyn E, et al. Among authors: bocian e. Med Wieku Rozwoj. 2003 Jul-Sep;7(3):389-401. Med Wieku Rozwoj. 2003. PMID: 14963346 Polish.

9

[Subtelomeric aberration as a cause of severe somatic and psychomotor retardation in a child with dysmorphic features and CNS defects].

Kutkowska-Kaźmierczak A, Obersztyn E, Helias-Rodzewicz Z, Bocian E, Mazurczak T. Kutkowska-Kaźmierczak A, et al. Among authors: bocian e. Med Wieku Rozwoj. 2004 Oct-Dec;8(4 Pt 1):949-62. Med Wieku Rozwoj. 2004. PMID: 15951614 Polish.

10

[Familial subtelomeric abnormality der(4)t(4p16.3;21q22.3) as a cause of mental retardation and mild dysmorphic features].

Obersztyn E, Klapecki J, Helias-Rodzewicz Z, Bocian E, Mazurczak T. Obersztyn E, et al. Among authors: bocian e. Med Wieku Rozwoj. 2006 Jan-Mar;10(1 Pt 2):199-209. Med Wieku Rozwoj. 2006. PMID: 17028389 Polish.

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