Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

H Rehder

Showing results (91-100 of 114) with videos related to

Pageof 12
Sort By:
Nature Genetics|September 1, 1993
The insulin-like growth factor type-2 receptor gene is imprinted in the mouse but not in humansV M Kalscheuer, E C Mariman, M T Schepens, et al.
Clinical Genetics|May 22, 2008
Dysmorphic syndrome of hereditary neuralgic amyotrophy associated with a SEPT9 gene mutation--a family studyF Laccone, M C Hannibal, J Neesen, et al.
European Journal of Human Genetics : EJHG|February 13, 2002
Low incidence of UPD in spontaneous abortions beyond the 5th gestational weekB Fritz, M Aslan, V Kalscheuer, et al.
American Journal of Medical Genetics|October 21, 1999
Somatic mosaicism of a greater than 1.7-Mb deletion of genomic DNA involving the entire NF1 gene as verified by FISH: further evidence for a contiguous gene syndrome in 17q11.2B Streubel, E Latta, H Kehrer-Sawatzki, et al.
American Journal of Medical Genetics|February 15, 1993
New autosomal recessive lethal disorder with polycystic kidneys type Potter I, characteristic face, microcephaly, brachymelia, and congenital heart defectsG Gillessen-Kaesbach, P Meinecke, C Garrett, et al.
Clinical Genetics|October 16, 2007
A disease causing deletion of 29 base pairs in intron 15 in the MKS1 gene is highly associated with the campomelic variant of the Meckel-Gruber syndromeB Auber, P Burfeind, S Herold, et al.
Prenatal Diagnosis|November 1, 1988
Cardiac defects in chromosomally abnormal human embryos of 10-14 weeks' gestationW Coerdt, H Rehder, H J Gebauer, et al.
Human Genetics|April 3, 2001
Marked differences in unilateral isolated retinoblastomas from young and older children studied by comparative genomic hybridizationS Herzog, D R Lohmann, K Buiting, et al.
Geburtshilfe Und Frauenheilkunde|December 1, 1991
[Diagnosis of fetal virus infections by in situ hybridization]Y Mehraein, H Rehder, H G Draeger, et al.
Fetal Diagnosis and Therapy|August 18, 2001
Duplication dup(1)(q32q44) detected by comparative genomic hybridization (CGH): further delineation of trisomies 1qC Bartsch, M Aslan, J Köhler, et al.
Pageof 12

Showing results (91-100 of 114) with videos related to

Sort By:
Pageof 12
Nature Genetics|September 1, 1993
The insulin-like growth factor type-2 receptor gene is imprinted in the mouse but not in humansV M Kalscheuer, E C Mariman, M T Schepens, et al.
Clinical Genetics|May 22, 2008
Dysmorphic syndrome of hereditary neuralgic amyotrophy associated with a SEPT9 gene mutation--a family studyF Laccone, M C Hannibal, J Neesen, et al.
European Journal of Human Genetics : EJHG|February 13, 2002
Low incidence of UPD in spontaneous abortions beyond the 5th gestational weekB Fritz, M Aslan, V Kalscheuer, et al.
American Journal of Medical Genetics|October 21, 1999
Somatic mosaicism of a greater than 1.7-Mb deletion of genomic DNA involving the entire NF1 gene as verified by FISH: further evidence for a contiguous gene syndrome in 17q11.2B Streubel, E Latta, H Kehrer-Sawatzki, et al.
American Journal of Medical Genetics|February 15, 1993
New autosomal recessive lethal disorder with polycystic kidneys type Potter I, characteristic face, microcephaly, brachymelia, and congenital heart defectsG Gillessen-Kaesbach, P Meinecke, C Garrett, et al.
Clinical Genetics|October 16, 2007
A disease causing deletion of 29 base pairs in intron 15 in the MKS1 gene is highly associated with the campomelic variant of the Meckel-Gruber syndromeB Auber, P Burfeind, S Herold, et al.
Prenatal Diagnosis|November 1, 1988
Cardiac defects in chromosomally abnormal human embryos of 10-14 weeks' gestationW Coerdt, H Rehder, H J Gebauer, et al.
Human Genetics|April 3, 2001
Marked differences in unilateral isolated retinoblastomas from young and older children studied by comparative genomic hybridizationS Herzog, D R Lohmann, K Buiting, et al.
Geburtshilfe Und Frauenheilkunde|December 1, 1991
[Diagnosis of fetal virus infections by in situ hybridization]Y Mehraein, H Rehder, H G Draeger, et al.
Fetal Diagnosis and Therapy|August 18, 2001
Duplication dup(1)(q32q44) detected by comparative genomic hybridization (CGH): further delineation of trisomies 1qC Bartsch, M Aslan, J Köhler, et al.
Pageof 12