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H Northrup

Showing results (61-70 of 68) with videos related to

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Nature Genetics|September 1, 1992
Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney diseaseR S Kandt, J L Haines, M Smith, et al.
American Journal of Human Genetics|October 11, 1992
Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhereH Northrup, D J Kwiatkowski, E S Roach, et al.
American Journal of Medical Genetics. Part A|November 12, 2005
Promotor genotype of the platelet-derived growth factor receptor-alpha gene shows population stratification but not association with spina bifida meningomyeloceleK-S Au, H Northrup, T J Kirkpatrick, et al.
American Journal of Medical Genetics|November 1, 1988
Prenatal detection of 46,XY,rec(5),dup q, inv(5)(p13q33) using DNA analysis, flow cytometry, and in situ hybridization to supplement classical cytogenetic analysisA O Martin, H Northrup, D H Ledbetter, et al.
Scientific Reports|February 12, 2021
Human myelomeningocele risk and ultra-rare deleterious variants in genes associated with cilium, WNT-signaling, ECM, cytoskeleton and cell migrationK S Au, L Hebert, P Hillman, et al.
Human Mutation|January 4, 2001
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathiesM M Sohocki, S P Daiger, S J Bowne, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 23, 2025
Morphometric analysis of spina bifida after fetal repair shows new subtypes with associated outcomesL K Mann, S Pandiri, N Agarwal, et al.
The American Journal of Pathology|August 4, 2001
The generation and characterization of a cell line derived from a sporadic renal angiomyolipoma: use of telomerase to obtain stable populations of cells from benign neoplasmsJ L Arbiser, R Yeung, S W Weiss, et al.
Pageof 7

Showing results (61-70 of 68) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 68 results.
Nature Genetics|September 1, 1992
Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney diseaseR S Kandt, J L Haines, M Smith, et al.
American Journal of Human Genetics|October 11, 1992
Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhereH Northrup, D J Kwiatkowski, E S Roach, et al.
American Journal of Medical Genetics. Part A|November 12, 2005
Promotor genotype of the platelet-derived growth factor receptor-alpha gene shows population stratification but not association with spina bifida meningomyeloceleK-S Au, H Northrup, T J Kirkpatrick, et al.
American Journal of Medical Genetics|November 1, 1988
Prenatal detection of 46,XY,rec(5),dup q, inv(5)(p13q33) using DNA analysis, flow cytometry, and in situ hybridization to supplement classical cytogenetic analysisA O Martin, H Northrup, D H Ledbetter, et al.
Scientific Reports|February 12, 2021
Human myelomeningocele risk and ultra-rare deleterious variants in genes associated with cilium, WNT-signaling, ECM, cytoskeleton and cell migrationK S Au, L Hebert, P Hillman, et al.
Human Mutation|January 4, 2001
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathiesM M Sohocki, S P Daiger, S J Bowne, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 23, 2025
Morphometric analysis of spina bifida after fetal repair shows new subtypes with associated outcomesL K Mann, S Pandiri, N Agarwal, et al.
The American Journal of Pathology|August 4, 2001
The generation and characterization of a cell line derived from a sporadic renal angiomyolipoma: use of telomerase to obtain stable populations of cells from benign neoplasmsJ L Arbiser, R Yeung, S W Weiss, et al.
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