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R P Erickson

Showing results (331-340 of 347) with videos related to

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American Journal of Medical Genetics|May 17, 1996
Molecular analysis in true hermaphrodites with different karyotypes and similar phenotypesL Torres, M López, J P Méndez, et al.
Journal of Molecular Biology|April 20, 1985
Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosomeJ Wolfe, S M Darling, R P Erickson, et al.
Lymphology|March 12, 2010
Lymphedema-distichiasis syndrome without FOXC2 mutation: evidence for chromosome 16 duplication upstream of FOXC2M H Witte, R P Erickson, M Khalil, et al.
American Journal of Human Genetics|November 15, 2000
Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndromeJ Fang, S L Dagenais, R P Erickson, et al.
Journal of Chromatography. A|April 23, 2005
Towards smaller and faster gas chromatography-mass spectrometry systems for field chemical detectionP A Smith, M T Sng, B A Eckenrode, et al.
American Journal of Human Genetics|July 1, 1985
HLA antigens, phytohemagglutinin stimulation, and corticosteroid responseR P Erickson, L A Heidel, J J Kapur, et al.
Clinical Genetics|July 13, 2012
X-linked CHARGE-like Abruzzo-Erickson syndrome and classic cleft palate with ankyloglossia result from TBX22 splicing mutationsE Pauws, E Peskett, C Boissin, et al.
The Journal of Allergy and Clinical Immunology|March 17, 2000
A cluster of seven tightly linked polymorphisms in the IL-13 gene is associated with total serum IgE levels in three populations of white childrenP E Graves, M Kabesch, M Halonen, et al.
Journal of Medical Genetics|September 1, 1987
Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8S R Diehl, M Boehnke, F S Collins, et al.
Human Molecular Genetics|February 28, 1998
Characterisation of the coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and mapping to the Sxrb interval of the mouse Y chromosome of the Dffry geneG M Brown, R A Furlong, C A Sargent, et al.
Pageof 35

Showing results (331-340 of 347) with videos related to

Sort By:
Pageof 35
American Journal of Medical Genetics|May 17, 1996
Molecular analysis in true hermaphrodites with different karyotypes and similar phenotypesL Torres, M López, J P Méndez, et al.
Journal of Molecular Biology|April 20, 1985
Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosomeJ Wolfe, S M Darling, R P Erickson, et al.
Lymphology|March 12, 2010
Lymphedema-distichiasis syndrome without FOXC2 mutation: evidence for chromosome 16 duplication upstream of FOXC2M H Witte, R P Erickson, M Khalil, et al.
American Journal of Human Genetics|November 15, 2000
Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndromeJ Fang, S L Dagenais, R P Erickson, et al.
Journal of Chromatography. A|April 23, 2005
Towards smaller and faster gas chromatography-mass spectrometry systems for field chemical detectionP A Smith, M T Sng, B A Eckenrode, et al.
American Journal of Human Genetics|July 1, 1985
HLA antigens, phytohemagglutinin stimulation, and corticosteroid responseR P Erickson, L A Heidel, J J Kapur, et al.
Clinical Genetics|July 13, 2012
X-linked CHARGE-like Abruzzo-Erickson syndrome and classic cleft palate with ankyloglossia result from TBX22 splicing mutationsE Pauws, E Peskett, C Boissin, et al.
The Journal of Allergy and Clinical Immunology|March 17, 2000
A cluster of seven tightly linked polymorphisms in the IL-13 gene is associated with total serum IgE levels in three populations of white childrenP E Graves, M Kabesch, M Halonen, et al.
Journal of Medical Genetics|September 1, 1987
Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8S R Diehl, M Boehnke, F S Collins, et al.
Human Molecular Genetics|February 28, 1998
Characterisation of the coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and mapping to the Sxrb interval of the mouse Y chromosome of the Dffry geneG M Brown, R A Furlong, C A Sargent, et al.
Pageof 35