A T Midro - JoVE Visualize

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Klinika Oczna|May 1, 1992

[Familial occurrence of congenital aniridia]R Zalewska, A T Midro, A Bakunowicz-Lazarczyk, et al.

Clinical Genetics|September 1, 1988

Familial occurrence of isodicentric X chromosomes with different breakpointsA T Midro, M Kulikowski, A Sawicka, et al.

Genomics|February 13, 2001

Construction of a detailed physical and transcript map of the candidate region for Russell-Silver syndrome on chromosome 17q23-q24S Dörr, A T Midro, C Färber, et al.

Genetic Counseling (Geneva, Switzerland)|April 23, 2005

A natural history of a child with monosomy 5p syndrome (Cat-cry/Cri-du-chat syndrome) during the 18 years of follow-upR Posmyk, B Panasiuk, S A Yatsenko, et al.

Ginekologia Polska|January 6, 2001

[Genetic risk of families with t(1;2)(q42;q33) GTG, RHG, QFQ, FISH]B Stasiewicz-Jarocka, B Raczkiewicz, D Kowalczyk, et al.

Ginekologia Polska|June 26, 1998

[Familial complex chromosome translocation of t(1;4;10)(q21.3;q27;q26.1) verified by FISH]A Sawicka, R Leśniewicz, M Zawada, et al.

Pediatria Polska|September 1, 1995

[Floating-Harbor syndrome in a girl with somatic asymmetry]A T Midro, M Rogowska, E Hubert, et al.

Ginekologia Polska|May 4, 1999

[Pedigree analysis of childless families of reciprocal chromosome translocation carriers]B Stasiewicz-Jarocka, B Panasiuk, A Sawicka, et al.

Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1990

[Sex chromosome aberrations in patients with menstruation disorders]A T Midro, B Panasiuk, J Radwan, et al.

Folia Histochemica Et Cytobiologica|May 26, 2001

Sequence polymorphisms of the EDA and the DL genes in the patients with an X-linked and an autosomal forms of anhidrotic ectodermal dysplasiaA Kobielak, K Kobielak, S A Wiśniewski, et al.

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Showing results (21-30 of 43) with videos related to

Sort By:

Pageof 5

Klinika Oczna|May 1, 1992

[Familial occurrence of congenital aniridia]R Zalewska, A T Midro, A Bakunowicz-Lazarczyk, et al.

Clinical Genetics|September 1, 1988

Familial occurrence of isodicentric X chromosomes with different breakpointsA T Midro, M Kulikowski, A Sawicka, et al.

Genomics|February 13, 2001

Construction of a detailed physical and transcript map of the candidate region for Russell-Silver syndrome on chromosome 17q23-q24S Dörr, A T Midro, C Färber, et al.

Genetic Counseling (Geneva, Switzerland)|April 23, 2005

A natural history of a child with monosomy 5p syndrome (Cat-cry/Cri-du-chat syndrome) during the 18 years of follow-upR Posmyk, B Panasiuk, S A Yatsenko, et al.

Ginekologia Polska|January 6, 2001

[Genetic risk of families with t(1;2)(q42;q33) GTG, RHG, QFQ, FISH]B Stasiewicz-Jarocka, B Raczkiewicz, D Kowalczyk, et al.

Ginekologia Polska|June 26, 1998

[Familial complex chromosome translocation of t(1;4;10)(q21.3;q27;q26.1) verified by FISH]A Sawicka, R Leśniewicz, M Zawada, et al.

Pediatria Polska|September 1, 1995

[Floating-Harbor syndrome in a girl with somatic asymmetry]A T Midro, M Rogowska, E Hubert, et al.

Ginekologia Polska|May 4, 1999

[Pedigree analysis of childless families of reciprocal chromosome translocation carriers]B Stasiewicz-Jarocka, B Panasiuk, A Sawicka, et al.

Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1990

[Sex chromosome aberrations in patients with menstruation disorders]A T Midro, B Panasiuk, J Radwan, et al.

Folia Histochemica Et Cytobiologica|May 26, 2001

Sequence polymorphisms of the EDA and the DL genes in the patients with an X-linked and an autosomal forms of anhidrotic ectodermal dysplasiaA Kobielak, K Kobielak, S A Wiśniewski, et al.

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