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I Kennerknecht

Showing results (31-40 of 44) with videos related to

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Human Reproduction (Oxford, England)|January 25, 2005
Mosaic status in lymphocytes of infertile men with or without Klinefelter syndromeP Lenz, C M Luetjens, A Kamischke, et al.
Prenatal Diagnosis|October 1, 1993
Cytogenetic diagnoses after chorionic villus sampling are less reliable in very-high-or very-low-risk pregnanciesI Kennerknecht, G Barbi, M Wolf, et al.
Prenatal Diagnosis|January 13, 1999
False-negative findings in chorionic villus sampling. An experimental approach and review of the literatureI Kennerknecht, G Barbi, M Djalali, et al.
Neurology|December 30, 2004
Familial aggregation of strong hemispheric language lateralizationK Anneken, C Konrad, B Dräger, et al.
American Journal of Medical Genetics|December 1, 1993
Familial occurrence of agonadism and multiple internal malformations in phenotypically normal girls with 46,XY and 46,XX karyotypes, respectively: a new autosomal recessive syndromeI Kennerknecht, W Sorgo, R Oberhoffer, et al.
Neuropediatrics|August 28, 2010
Neurological manifestations in individuals with pure cutaneous or syndromic (Ruggieri-Happle syndrome) phenotypes with "cutis tricolor": a study of 14 casesE Lionetti, P Pavone, I Kennerknecht, et al.
American Journal of Medical Genetics|June 27, 1997
XX-agonadism in a fetus with multiple dysraphic lesions: a new syndromeI Kennerknecht, T Mattfeldt, W Paulus, et al.
Journal of Medical Genetics|July 1, 1997
A case of apparent trisomy 21 without the Down's syndrome phenotypeD Avramopoulos, I Kennerknecht, G Barbi, et al.
Journal of Neurology|December 2, 2010
Congenital prosopagnosia: multistage anatomical and functional deficits in face processing circuitryV Dinkelacker, M Grüter, P Klaver, et al.
Molecular Biology and Evolution|July 16, 2004
PCR-induced sequence alterations hamper the typing of prehistoric bone samples for diagnostic achondroplasia mutationsC M Pusch, M Broghammer, G J Nicholson, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Human Reproduction (Oxford, England)|January 25, 2005
Mosaic status in lymphocytes of infertile men with or without Klinefelter syndromeP Lenz, C M Luetjens, A Kamischke, et al.
Prenatal Diagnosis|October 1, 1993
Cytogenetic diagnoses after chorionic villus sampling are less reliable in very-high-or very-low-risk pregnanciesI Kennerknecht, G Barbi, M Wolf, et al.
Prenatal Diagnosis|January 13, 1999
False-negative findings in chorionic villus sampling. An experimental approach and review of the literatureI Kennerknecht, G Barbi, M Djalali, et al.
Neurology|December 30, 2004
Familial aggregation of strong hemispheric language lateralizationK Anneken, C Konrad, B Dräger, et al.
American Journal of Medical Genetics|December 1, 1993
Familial occurrence of agonadism and multiple internal malformations in phenotypically normal girls with 46,XY and 46,XX karyotypes, respectively: a new autosomal recessive syndromeI Kennerknecht, W Sorgo, R Oberhoffer, et al.
Neuropediatrics|August 28, 2010
Neurological manifestations in individuals with pure cutaneous or syndromic (Ruggieri-Happle syndrome) phenotypes with "cutis tricolor": a study of 14 casesE Lionetti, P Pavone, I Kennerknecht, et al.
American Journal of Medical Genetics|June 27, 1997
XX-agonadism in a fetus with multiple dysraphic lesions: a new syndromeI Kennerknecht, T Mattfeldt, W Paulus, et al.
Journal of Medical Genetics|July 1, 1997
A case of apparent trisomy 21 without the Down's syndrome phenotypeD Avramopoulos, I Kennerknecht, G Barbi, et al.
Journal of Neurology|December 2, 2010
Congenital prosopagnosia: multistage anatomical and functional deficits in face processing circuitryV Dinkelacker, M Grüter, P Klaver, et al.
Molecular Biology and Evolution|July 16, 2004
PCR-induced sequence alterations hamper the typing of prehistoric bone samples for diagnostic achondroplasia mutationsC M Pusch, M Broghammer, G J Nicholson, et al.
Pageof 5