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P Wieacker

Showing results (91-100 of 105) with videos related to

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Human Genetics|January 1, 1983
Regional localization of the human factor IX gene by molecular hybridizationP F Chance, K A Dyer, K Kurachi, et al.
Klinische Padiatrie|January 1, 1999
[Multiplication of chromosomes and primary leucocyte number in childhood ALL and hyperdiploid karyotype]E Bannier, B Degen, U Mittler, et al.
Human Reproduction (Oxford, England)|July 13, 1999
Frequency of CFTR gene mutations in males participating in an ICSI programmeS Jakubiczka, T Bettecken, M Stumm, et al.
American Journal of Human Genetics|March 1, 1984
Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybridsP Wieacker, K E Davies, H J Cooke, et al.
Clinical Genetics|March 1, 1985
Norrie's disease: close linkage with genetic markers from the proximal short arm of the X chromosomeA Gal, C Stolzenberger, T Wienker, et al.
The Journal of Clinical Endocrinology and Metabolism|April 22, 2011
Analysis of the Wilms' tumor suppressor gene (WT1) in patients 46,XY disorders of sex developmentB Köhler, H Biebermann, V Friedsam, et al.
Clinical Genetics|November 28, 2015
Mutations in WNT9B are associated with Mayer-Rokitansky-Küster-Hauser syndromeD E J Waschk, A-C Tewes, T Römer, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
A new variant of Zellweger syndrome with normal peroxisomal functions in cultured fibroblastsR B Schutgens, R J Wanders, C Jakobs, et al.
Clinical Genetics|October 19, 2007
Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndromeI Wieland, C Weidner, R Ciccone, et al.
Leukemia|September 20, 2013
Molecular monitoring in NUP214-ABL-positive T-acute lymphoblastic leukemia reveals clonal diversity and helps to guide targeted therapyS Koschmieder, T Burmeister, M Brüggemann, et al.
Pageof 11

Showing results (91-100 of 105) with videos related to

Sort By:
Pageof 11
Human Genetics|January 1, 1983
Regional localization of the human factor IX gene by molecular hybridizationP F Chance, K A Dyer, K Kurachi, et al.
Klinische Padiatrie|January 1, 1999
[Multiplication of chromosomes and primary leucocyte number in childhood ALL and hyperdiploid karyotype]E Bannier, B Degen, U Mittler, et al.
Human Reproduction (Oxford, England)|July 13, 1999
Frequency of CFTR gene mutations in males participating in an ICSI programmeS Jakubiczka, T Bettecken, M Stumm, et al.
American Journal of Human Genetics|March 1, 1984
Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybridsP Wieacker, K E Davies, H J Cooke, et al.
Clinical Genetics|March 1, 1985
Norrie's disease: close linkage with genetic markers from the proximal short arm of the X chromosomeA Gal, C Stolzenberger, T Wienker, et al.
The Journal of Clinical Endocrinology and Metabolism|April 22, 2011
Analysis of the Wilms' tumor suppressor gene (WT1) in patients 46,XY disorders of sex developmentB Köhler, H Biebermann, V Friedsam, et al.
Clinical Genetics|November 28, 2015
Mutations in WNT9B are associated with Mayer-Rokitansky-Küster-Hauser syndromeD E J Waschk, A-C Tewes, T Römer, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
A new variant of Zellweger syndrome with normal peroxisomal functions in cultured fibroblastsR B Schutgens, R J Wanders, C Jakobs, et al.
Clinical Genetics|October 19, 2007
Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndromeI Wieland, C Weidner, R Ciccone, et al.
Leukemia|September 20, 2013
Molecular monitoring in NUP214-ABL-positive T-acute lymphoblastic leukemia reveals clonal diversity and helps to guide targeted therapyS Koschmieder, T Burmeister, M Brüggemann, et al.
Pageof 11