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P Papenhausen

Showing results (21-30 of 25) with videos related to

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The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 24, 2004
Twin-twin transfusion syndrome in a dizygotic monochorionic-diamniotic twin pregnancyR A Quintero, O T Mueller, J M Martínez, et al.
Journal of Medical Genetics|October 4, 2005
Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilitiesJ B Ravnan, J H Tepperberg, P Papenhausen, et al.
Blood|October 1, 1987
HL-T, a new cell line derived from HL-60 promyelocytic leukemia cell cultures expressing terminal transferase and secreting suppressor activityE Paietta, R J Stockert, T Calvelli, et al.
The Journal of Clinical Endocrinology and Metabolism|December 12, 2001
Phenotypes Associated with SHOX DeficiencyJ L Ross, C Scott, P Marttila, et al.
Human Genetics|January 24, 1998
Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalitiesE Schröck, T Veldman, H Padilla-Nash, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 24, 2004
Twin-twin transfusion syndrome in a dizygotic monochorionic-diamniotic twin pregnancyR A Quintero, O T Mueller, J M Martínez, et al.
Journal of Medical Genetics|October 4, 2005
Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilitiesJ B Ravnan, J H Tepperberg, P Papenhausen, et al.
Blood|October 1, 1987
HL-T, a new cell line derived from HL-60 promyelocytic leukemia cell cultures expressing terminal transferase and secreting suppressor activityE Paietta, R J Stockert, T Calvelli, et al.
The Journal of Clinical Endocrinology and Metabolism|December 12, 2001
Phenotypes Associated with SHOX DeficiencyJ L Ross, C Scott, P Marttila, et al.
Human Genetics|January 24, 1998
Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalitiesE Schröck, T Veldman, H Padilla-Nash, et al.
Pageof 3