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Marjorie Withers

Showing results (1-10 of 19) with videos related to

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Work (Reading, Mass.)|February 13, 2015
Bridging the gaps: An early integrated support collaborative for at risk mothers in rural MaineJennifer Morton, Marjorie Withers, Shelley Cohen Konrad, et al.
Genome Research|November 3, 2004
Serial segmental duplications during primate evolution result in complex human genome architecturePawełl Stankiewicz, Christine J Shaw, Marjorie Withers, et al.
American Journal of Human Genetics|October 11, 2011
Frequency of nonallelic homologous recombination is correlated with length of homology: evidence that ectopic synapsis precedes ectopic crossing-overPengfei Liu, Melanie Lacaria, Feng Zhang, et al.
American Journal of Human Genetics|March 22, 2003
Genome architecture catalyzes nonrecurrent chromosomal rearrangementsPaweł Stankiewicz, Christine J Shaw, Jason D Dapper, et al.
American Journal of Medical Genetics. Part A|June 14, 2006
Mutational and genotype-phenotype correlation analyses in 28 Polish patients with Cornelia de Lange syndromeJiong Yan, Gulam Mustafa Saifi, Tomasz H Wierzba, et al.
Plos Genetics|July 31, 2007
Population bottlenecks as a potential major shaping force of human genome architectureAdrian Gherman, Peter E Chen, Tanya M Teslovich, et al.
The Journal of Allergy and Clinical Immunology|April 26, 2011
Transmembrane activator and CAML interactor (TACI) haploinsufficiency results in B-cell dysfunction in patients with Smith-Magenis syndromeJavier Chinen, Monica Martinez-Gallo, Wenli Gu, et al.
American Journal of Human Genetics|February 24, 2005
Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasiaGopalrao V N Velagaleti, Gabriel A Bien-Willner, Jill K Northup, et al.
The Journal of Clinical Endocrinology and Metabolism|October 17, 2014
Whole-exome sequencing identifies homozygous GPR161 mutation in a family with pituitary stalk interruption syndromeEnder Karaca, Ramazan Buyukkaya, Davut Pehlivan, et al.
American Journal of Human Genetics|March 1, 2016
DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow SyndromeJanson J White, Juliana F Mazzeu, Alexander Hoischen, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Work (Reading, Mass.)|February 13, 2015
Bridging the gaps: An early integrated support collaborative for at risk mothers in rural MaineJennifer Morton, Marjorie Withers, Shelley Cohen Konrad, et al.
Genome Research|November 3, 2004
Serial segmental duplications during primate evolution result in complex human genome architecturePawełl Stankiewicz, Christine J Shaw, Marjorie Withers, et al.
American Journal of Human Genetics|October 11, 2011
Frequency of nonallelic homologous recombination is correlated with length of homology: evidence that ectopic synapsis precedes ectopic crossing-overPengfei Liu, Melanie Lacaria, Feng Zhang, et al.
American Journal of Human Genetics|March 22, 2003
Genome architecture catalyzes nonrecurrent chromosomal rearrangementsPaweł Stankiewicz, Christine J Shaw, Jason D Dapper, et al.
American Journal of Medical Genetics. Part A|June 14, 2006
Mutational and genotype-phenotype correlation analyses in 28 Polish patients with Cornelia de Lange syndromeJiong Yan, Gulam Mustafa Saifi, Tomasz H Wierzba, et al.
Plos Genetics|July 31, 2007
Population bottlenecks as a potential major shaping force of human genome architectureAdrian Gherman, Peter E Chen, Tanya M Teslovich, et al.
The Journal of Allergy and Clinical Immunology|April 26, 2011
Transmembrane activator and CAML interactor (TACI) haploinsufficiency results in B-cell dysfunction in patients with Smith-Magenis syndromeJavier Chinen, Monica Martinez-Gallo, Wenli Gu, et al.
American Journal of Human Genetics|February 24, 2005
Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasiaGopalrao V N Velagaleti, Gabriel A Bien-Willner, Jill K Northup, et al.
The Journal of Clinical Endocrinology and Metabolism|October 17, 2014
Whole-exome sequencing identifies homozygous GPR161 mutation in a family with pituitary stalk interruption syndromeEnder Karaca, Ramazan Buyukkaya, Davut Pehlivan, et al.
American Journal of Human Genetics|March 1, 2016
DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow SyndromeJanson J White, Juliana F Mazzeu, Alexander Hoischen, et al.
Pageof 2