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Showing results (31-40 of 53) with videos related to

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American Journal of Medical Genetics|July 15, 1994
Improved sizing of fragile X CCG repeats by nested polymerase chain reactionG Levinson, A Maddalena, F T Palmer, et al.
Journal of Applied Crystallography|June 7, 2014
Magnetic field dependent small-angle neutron scattering on a Co nanorod array: evidence for intraparticle spin misalignmentA Günther, J-P Bick, P Szary, et al.
Journal of Pediatric Genetics|February 15, 2018
A Rare Combination of Functional Disomy Xp, Deletion Xq13.2-q28 Spanning the <i>XIST</i> Gene, and Duplication 3q25.33-q29 in a Female with der(X)t(X;3)(q13.2;q25.33)Jess F Peterson, Donald G Basel, David P Bick, et al.
American Journal of Medical Genetics. Part A|October 4, 2005
Interstitial deletion of chromosome 12q: genotype-phenotype correlation of two patients utilizing array comparative genomic hybridizationOphir D Klein, Philip D Cotter, Ann M Schmidt, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2010
A timely arrival for genomic medicineAlan N Mayer, David P Dimmock, Marjorie J Arca, et al.
American Journal of Medical Genetics|July 12, 1996
Molecular fragile X screening in normal populationsW C Spence, S H Black, L Fallon, et al.
Journal of Medical Genetics|November 14, 2006
Zoom-in comparative genomic hybridisation arrays for the characterisation of variable breakpoint contiguous gene syndromesJennifer J Johnston, Robert L Walker, Sean Davis, et al.
American Journal of Medical Genetics. Part A|August 24, 2016
Concomitant 11p15.4-p15.5 duplication and terminal 22q13.33 deletion in a patient with features of Beckwith-Wiedemann syndromeJess F Peterson, David P Bick, Gabrielle C Geddes, et al.
Clinical Endocrinology|December 18, 2003
Analysis of the PROP1 gene in a large cohort of patients with idiopathic hypogonadotropic hypogonadismJohn K Park, Metin Ozata, Lynn P Chorich, et al.
The Journal of Investigative Dermatology|July 26, 2013
AKT1 gene mutation levels are correlated with the type of dermatologic lesions in patients with Proteus syndromeMarjorie J Lindhurst, Ji-An Wang, Hadley M Bloomhardt, et al.
Pageof 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics|July 15, 1994
Improved sizing of fragile X CCG repeats by nested polymerase chain reactionG Levinson, A Maddalena, F T Palmer, et al.
Journal of Applied Crystallography|June 7, 2014
Magnetic field dependent small-angle neutron scattering on a Co nanorod array: evidence for intraparticle spin misalignmentA Günther, J-P Bick, P Szary, et al.
Journal of Pediatric Genetics|February 15, 2018
A Rare Combination of Functional Disomy Xp, Deletion Xq13.2-q28 Spanning the <i>XIST</i> Gene, and Duplication 3q25.33-q29 in a Female with der(X)t(X;3)(q13.2;q25.33)Jess F Peterson, Donald G Basel, David P Bick, et al.
American Journal of Medical Genetics. Part A|October 4, 2005
Interstitial deletion of chromosome 12q: genotype-phenotype correlation of two patients utilizing array comparative genomic hybridizationOphir D Klein, Philip D Cotter, Ann M Schmidt, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2010
A timely arrival for genomic medicineAlan N Mayer, David P Dimmock, Marjorie J Arca, et al.
American Journal of Medical Genetics|July 12, 1996
Molecular fragile X screening in normal populationsW C Spence, S H Black, L Fallon, et al.
Journal of Medical Genetics|November 14, 2006
Zoom-in comparative genomic hybridisation arrays for the characterisation of variable breakpoint contiguous gene syndromesJennifer J Johnston, Robert L Walker, Sean Davis, et al.
American Journal of Medical Genetics. Part A|August 24, 2016
Concomitant 11p15.4-p15.5 duplication and terminal 22q13.33 deletion in a patient with features of Beckwith-Wiedemann syndromeJess F Peterson, David P Bick, Gabrielle C Geddes, et al.
Clinical Endocrinology|December 18, 2003
Analysis of the PROP1 gene in a large cohort of patients with idiopathic hypogonadotropic hypogonadismJohn K Park, Metin Ozata, Lynn P Chorich, et al.
The Journal of Investigative Dermatology|July 26, 2013
AKT1 gene mutation levels are correlated with the type of dermatologic lesions in patients with Proteus syndromeMarjorie J Lindhurst, Ji-An Wang, Hadley M Bloomhardt, et al.
Pageof 6