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K Sperling

Showing results (101-110 of 145) with videos related to

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Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|November 1, 1993
Oocytes from pachytene to dictyotene can easily be analysed in neonatal rodentsA P Singh, S Maerzke, O von Deimling, et al.
Human Molecular Genetics|August 1, 1995
Recurrent nasal polyps as a monosymptomatic form of cystic fibrosis associated with a novel in-frame deletion (591del18) in the CFTR geneR Varon, K Magdorf, D Staab, et al.
Human Genetics|January 1, 1982
Rabl's model of the interphase chromosome arrangement tested in Chinese hamster cells by premature chromosome condensation and laser-UV-microbeam experimentsT Cremer, C Cremer, H Baumann, et al.
Clinical Genetics|February 1, 1991
Routine applications of DNA fingerprinting with the oligonucleotide probe (CAC)5/(GTG)5H Neitzel, M Digweed, P Nürnberg, et al.
European Journal of Pediatrics|August 23, 1977
Familial trisomy 9p and spinal muscular atrophy: clinical, cytogenetic and embryological findingsM Tolksdorf, J Kunze, G Gross-Selbeck, et al.
American Journal of Human Genetics|July 1, 1997
Different mechanisms and recurrence risks of imprinting defects in Angelman syndromeJ Bürger, K Buiting, B Dittrich, et al.
Journal of Medical Genetics|June 27, 2001
A unique form of autosomal dominant cataract explained by gene conversion between beta-crystallin B2 and its pseudogeneVanita, V Sarhadi, A Reis, et al.
Acta Anthropogenetica|January 1, 1983
H-Y antigen in human X-autosome translocationsA Mayerova, O Zuffardi, P Maraschio, et al.
Journal of Medical Genetics|July 22, 2005
Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instabilityE Seemanová, K Sperling, H Neitzel, et al.
Clinical Physiology (Oxford, England)|September 6, 2000
Regional cerebral blood flow during hyperventilation in patients with acute bacterial meningitisK Møller, P Høgh, F S Larsen, et al.
Pageof 15

Showing results (101-110 of 145) with videos related to

Sort By:
Pageof 15
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|November 1, 1993
Oocytes from pachytene to dictyotene can easily be analysed in neonatal rodentsA P Singh, S Maerzke, O von Deimling, et al.
Human Molecular Genetics|August 1, 1995
Recurrent nasal polyps as a monosymptomatic form of cystic fibrosis associated with a novel in-frame deletion (591del18) in the CFTR geneR Varon, K Magdorf, D Staab, et al.
Human Genetics|January 1, 1982
Rabl's model of the interphase chromosome arrangement tested in Chinese hamster cells by premature chromosome condensation and laser-UV-microbeam experimentsT Cremer, C Cremer, H Baumann, et al.
Clinical Genetics|February 1, 1991
Routine applications of DNA fingerprinting with the oligonucleotide probe (CAC)5/(GTG)5H Neitzel, M Digweed, P Nürnberg, et al.
European Journal of Pediatrics|August 23, 1977
Familial trisomy 9p and spinal muscular atrophy: clinical, cytogenetic and embryological findingsM Tolksdorf, J Kunze, G Gross-Selbeck, et al.
American Journal of Human Genetics|July 1, 1997
Different mechanisms and recurrence risks of imprinting defects in Angelman syndromeJ Bürger, K Buiting, B Dittrich, et al.
Journal of Medical Genetics|June 27, 2001
A unique form of autosomal dominant cataract explained by gene conversion between beta-crystallin B2 and its pseudogeneVanita, V Sarhadi, A Reis, et al.
Acta Anthropogenetica|January 1, 1983
H-Y antigen in human X-autosome translocationsA Mayerova, O Zuffardi, P Maraschio, et al.
Journal of Medical Genetics|July 22, 2005
Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instabilityE Seemanová, K Sperling, H Neitzel, et al.
Clinical Physiology (Oxford, England)|September 6, 2000
Regional cerebral blood flow during hyperventilation in patients with acute bacterial meningitisK Møller, P Høgh, F S Larsen, et al.
Pageof 15