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Showing results (191-200 of 278) with videos related to

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Human Reproduction (Oxford, England)|June 30, 2000
Non-reproductive heritable disorders in infertile couples and their first degree relativesD Meschede, B Lemcke, H M Behre, et al.
Prenatal Diagnosis|October 1, 1988
False negative cytogenetic result in direct preparations after CVSP Miny, S Basaran, W Holzgreve, et al.
Clinical Dysmorphology|July 1, 1996
Yunis-Varon syndrome: the first case of German originH Rabe, T Brune, R Rossi, et al.
Fertility and Sterility|June 17, 2000
Seminal plasma characteristics as indicators of cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in men with obstructive azoospermiaS von Eckardstein, T G Cooper, K Rutscha, et al.
Clinical Genetics|August 1, 1995
Congenital heart disease in the 48,XXYY syndromeD Meschede, T Nekarda, D Kececioglu, et al.
Human Reproduction (Oxford, England)|July 28, 2001
Low-level sex chromosome mosaicism in female partners of couples undergoing ICSI therapy does not significantly affect treatment outcomeB Sonntag, D Meschede, V Ullmann, et al.
Journal of Medical Genetics|December 1, 1990
Classical phenylketonuria in Bulgaria: RFLP haplotypes and frequency of the major mutationsL Kalaydjieva, B Dworniczak, C Aulehla-Scholz, et al.
Lancet (London, England)|February 11, 1989
Direct sequencing of amplified DNA in prenatal diagnosis of beta-thalassaemiaC Aulehla-Scholz, R Spiegelberg, P Miny, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Comparison of conformation-sensitive gel electrophoresis and single-strand conformation polymorphism analysis for detection of mutations in the BRCA1 gene using optimized conformation analysis protocolsA Markoff, H Sormbroen, N Bogdanova, et al.
American Journal of Medical Genetics|May 1, 1989
Validity of cytogenetic analyses from trophoblast tissue throughout gestationP Miny, S Basaran, I H Pawlowitzki, et al.
Pageof 28

Showing results (191-200 of 278) with videos related to

Sort By:
Pageof 28
Human Reproduction (Oxford, England)|June 30, 2000
Non-reproductive heritable disorders in infertile couples and their first degree relativesD Meschede, B Lemcke, H M Behre, et al.
Prenatal Diagnosis|October 1, 1988
False negative cytogenetic result in direct preparations after CVSP Miny, S Basaran, W Holzgreve, et al.
Clinical Dysmorphology|July 1, 1996
Yunis-Varon syndrome: the first case of German originH Rabe, T Brune, R Rossi, et al.
Fertility and Sterility|June 17, 2000
Seminal plasma characteristics as indicators of cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in men with obstructive azoospermiaS von Eckardstein, T G Cooper, K Rutscha, et al.
Clinical Genetics|August 1, 1995
Congenital heart disease in the 48,XXYY syndromeD Meschede, T Nekarda, D Kececioglu, et al.
Human Reproduction (Oxford, England)|July 28, 2001
Low-level sex chromosome mosaicism in female partners of couples undergoing ICSI therapy does not significantly affect treatment outcomeB Sonntag, D Meschede, V Ullmann, et al.
Journal of Medical Genetics|December 1, 1990
Classical phenylketonuria in Bulgaria: RFLP haplotypes and frequency of the major mutationsL Kalaydjieva, B Dworniczak, C Aulehla-Scholz, et al.
Lancet (London, England)|February 11, 1989
Direct sequencing of amplified DNA in prenatal diagnosis of beta-thalassaemiaC Aulehla-Scholz, R Spiegelberg, P Miny, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Comparison of conformation-sensitive gel electrophoresis and single-strand conformation polymorphism analysis for detection of mutations in the BRCA1 gene using optimized conformation analysis protocolsA Markoff, H Sormbroen, N Bogdanova, et al.
American Journal of Medical Genetics|May 1, 1989
Validity of cytogenetic analyses from trophoblast tissue throughout gestationP Miny, S Basaran, I H Pawlowitzki, et al.
Pageof 28