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S T Warren

Showing results (101-110 of 108) with videos related to

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Genomics|October 1, 1990
Assignment of X-linked hydrocephalus to Xq28 by linkage analysisP J Willems, I Dijkstra, B J Van der Auwera, et al.
Journal of Medical Genetics|December 10, 1997
Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locusM Losekoot, E Hoogendoorn, R Olmer, et al.
Cell|November 24, 2001
Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndromeV Brown, P Jin, S Ceman, et al.
Human Molecular Genetics|November 13, 1998
Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1C Gunter, W Paradee, D C Crawford, et al.
Genomics|August 1, 1992
Colocalization of the gene for nephrogenic diabetes insipidus (DIR) and the vasopressin type 2 receptor gene (AVPR2) in the Xq28 regionA M van den Ouweland, M T Knoop, V V Knoers, et al.
Journal of Medical Genetics|February 1, 1993
The fragile X syndrome: no evidence for any recent mutationsA P Smits, J C Dreesen, J G Post, et al.
Journal of Thrombosis and Haemostasis : JTH|July 15, 2006
Genetic determinants of normal variation in coagulation factor (F) IX levels: genome-wide scan and examination of the FIX structural geneM Khachidze, A Buil, K R Viel, et al.
American Journal of Human Genetics|March 21, 2000
Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American populationD C Crawford, C E Schwartz, K L Meadows, et al.
Pageof 11

Showing results (101-110 of 108) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 108 results.
Genomics|October 1, 1990
Assignment of X-linked hydrocephalus to Xq28 by linkage analysisP J Willems, I Dijkstra, B J Van der Auwera, et al.
Journal of Medical Genetics|December 10, 1997
Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locusM Losekoot, E Hoogendoorn, R Olmer, et al.
Cell|November 24, 2001
Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndromeV Brown, P Jin, S Ceman, et al.
Human Molecular Genetics|November 13, 1998
Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1C Gunter, W Paradee, D C Crawford, et al.
Genomics|August 1, 1992
Colocalization of the gene for nephrogenic diabetes insipidus (DIR) and the vasopressin type 2 receptor gene (AVPR2) in the Xq28 regionA M van den Ouweland, M T Knoop, V V Knoers, et al.
Journal of Medical Genetics|February 1, 1993
The fragile X syndrome: no evidence for any recent mutationsA P Smits, J C Dreesen, J G Post, et al.
Journal of Thrombosis and Haemostasis : JTH|July 15, 2006
Genetic determinants of normal variation in coagulation factor (F) IX levels: genome-wide scan and examination of the FIX structural geneM Khachidze, A Buil, K R Viel, et al.
American Journal of Human Genetics|March 21, 2000
Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American populationD C Crawford, C E Schwartz, K L Meadows, et al.
Pageof 11