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L G Shaffer

Showing results (91-100 of 133) with videos related to

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American Journal of Medical Genetics|August 8, 1997
Severe clinical phenotype due to an interstitial deletion of the short arm of chromosome 1: a brief reviewD W Stockton, H L Ross, C A Bacino, et al.
American Journal of Human Genetics|June 19, 1998
Paternal isodisomy of chromosome 7 associated with complete situs inversus and immotile ciliaY Pan, C D McCaskill, K H Thompson, et al.
Prenatal Diagnosis|September 6, 2001
Prenatal diagnosis of a homologous Robertsonian translocation involving chromosome 15D J Abrams, A R Aronoff, S Ann Berend, et al.
Prenatal Diagnosis|October 1, 1996
Analysis of nine pregnancies with confined placental mosaicism for trisomy 2L G Shaffer, S Langlois, C McCaskill, et al.
American Journal of Medical Genetics|April 15, 2000
Identification of Y chromatin directly in gonadal tissue by fluorescence in situ hybridization (FISH): significance for Ullrich-Turner syndrome screening in the cytogenetics laboratoryK E Atkins, A Gregg, A S Spikes, et al.
Prenatal Diagnosis|January 12, 2002
Prenatal interphase FISH diagnosis of PLP1 duplication associated with Pelizaeus-Merzbacher diseaseK Inoue, M Kanai, Y Tanabe, et al.
Archives of Neurology|October 27, 2001
Hereditary neuropathy with liability to pressure palsies is not a major cause of idiopathic carpal tunnel syndromeD W Stockton, R A Meade, D T Netscher, et al.
American Journal of Medical Genetics|November 20, 1995
Apparent mosaicism for del(17)(p11.2) ruled out by fluorescence in situ hybridization in a Smith-Magenis syndrome patientR C Juyal, B Finucane, L G Shaffer, et al.
Clinical Genetics|September 25, 2008
Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2B C Ballif, A Theisen, D M McDonald-McGinn, et al.
American Journal of Medical Genetics|April 15, 2000
Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II lociS A Berend, A S Spikes, C D Kashork, et al.
Pageof 14

Showing results (91-100 of 133) with videos related to

Sort By:
Pageof 14
American Journal of Medical Genetics|August 8, 1997
Severe clinical phenotype due to an interstitial deletion of the short arm of chromosome 1: a brief reviewD W Stockton, H L Ross, C A Bacino, et al.
American Journal of Human Genetics|June 19, 1998
Paternal isodisomy of chromosome 7 associated with complete situs inversus and immotile ciliaY Pan, C D McCaskill, K H Thompson, et al.
Prenatal Diagnosis|September 6, 2001
Prenatal diagnosis of a homologous Robertsonian translocation involving chromosome 15D J Abrams, A R Aronoff, S Ann Berend, et al.
Prenatal Diagnosis|October 1, 1996
Analysis of nine pregnancies with confined placental mosaicism for trisomy 2L G Shaffer, S Langlois, C McCaskill, et al.
American Journal of Medical Genetics|April 15, 2000
Identification of Y chromatin directly in gonadal tissue by fluorescence in situ hybridization (FISH): significance for Ullrich-Turner syndrome screening in the cytogenetics laboratoryK E Atkins, A Gregg, A S Spikes, et al.
Prenatal Diagnosis|January 12, 2002
Prenatal interphase FISH diagnosis of PLP1 duplication associated with Pelizaeus-Merzbacher diseaseK Inoue, M Kanai, Y Tanabe, et al.
Archives of Neurology|October 27, 2001
Hereditary neuropathy with liability to pressure palsies is not a major cause of idiopathic carpal tunnel syndromeD W Stockton, R A Meade, D T Netscher, et al.
American Journal of Medical Genetics|November 20, 1995
Apparent mosaicism for del(17)(p11.2) ruled out by fluorescence in situ hybridization in a Smith-Magenis syndrome patientR C Juyal, B Finucane, L G Shaffer, et al.
Clinical Genetics|September 25, 2008
Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2B C Ballif, A Theisen, D M McDonald-McGinn, et al.
American Journal of Medical Genetics|April 15, 2000
Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II lociS A Berend, A S Spikes, C D Kashork, et al.
Pageof 14