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Current Opinion in Endocrinology, Diabetes, and Obesity
|
April 15, 2015
Screening for Klinefelter syndrome
Amy S Herlihy, Robert I McLachlan
Acta Paediatrica (Oslo, Norway : 1992)
|
January 14, 2011
Postnatal screening for Klinefelter syndrome: is there a rationale?
Amy S Herlihy, Lynn Gillam, Jane L Halliday, et al.
The Medical Journal of Australia
|
April 1, 2011
The prevalence and diagnosis rates of Klinefelter syndrome: an Australian comparison
Amy S Herlihy, Jane L Halliday, Megan L Cock, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 7, 2011
The psychosocial impact of Klinefelter syndrome and factors influencing quality of life
Amy S Herlihy, Robert I McLachlan, Lynn Gillam, et al.
International Journal of Molecular Sciences
|
September 29, 2018
Expression of the <i>O</i>-Glycosylation Enzyme GalNAc-T3 in the Equatorial Segment Correlates with the Quality of Spermatozoa
Marie B Nygaard, Amy S Herlihy, Charlotte Jeanneau, et al.
Virchows Archiv : an International Journal of Pathology
|
June 1, 2006
Identity of M2A (D2-40) antigen and gp36 (Aggrus, T1A-2, podoplanin) in human developing testis, testicular carcinoma in situ and germ-cell tumours
Si Brask Sonne, Amy S Herlihy, Christina E Hoei-Hansen, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica
|
August 16, 2006
CDH1 (E-cadherin) in testicular germ cell neoplasia: suppressed translation of mRNA in pre-invasive carcinoma in situ but increased protein levels in advanced tumours
Si B Sonne, Christina E Hoei-Hansen, John E Nielsen, et al.
Expert Reviews in Molecular Medicine
|
July 2, 2015
Detection of skewed X-chromosome inactivation in Fragile X syndrome and X chromosome aneuploidy using quantitative melt analysis
David E Godler, Yoshimi Inaba, Charles E Schwartz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 13, 2012
Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study
Yoshimi Inaba, Amy S Herlihy, Charles E Schwartz, et al.
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of 1
Search research articles
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Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Current Opinion in Endocrinology, Diabetes, and Obesity
|
April 15, 2015
Screening for Klinefelter syndrome
Amy S Herlihy, Robert I McLachlan
Acta Paediatrica (Oslo, Norway : 1992)
|
January 14, 2011
Postnatal screening for Klinefelter syndrome: is there a rationale?
Amy S Herlihy, Lynn Gillam, Jane L Halliday, et al.
The Medical Journal of Australia
|
April 1, 2011
The prevalence and diagnosis rates of Klinefelter syndrome: an Australian comparison
Amy S Herlihy, Jane L Halliday, Megan L Cock, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 7, 2011
The psychosocial impact of Klinefelter syndrome and factors influencing quality of life
Amy S Herlihy, Robert I McLachlan, Lynn Gillam, et al.
International Journal of Molecular Sciences
|
September 29, 2018
Expression of the <i>O</i>-Glycosylation Enzyme GalNAc-T3 in the Equatorial Segment Correlates with the Quality of Spermatozoa
Marie B Nygaard, Amy S Herlihy, Charlotte Jeanneau, et al.
Virchows Archiv : an International Journal of Pathology
|
June 1, 2006
Identity of M2A (D2-40) antigen and gp36 (Aggrus, T1A-2, podoplanin) in human developing testis, testicular carcinoma in situ and germ-cell tumours
Si Brask Sonne, Amy S Herlihy, Christina E Hoei-Hansen, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica
|
August 16, 2006
CDH1 (E-cadherin) in testicular germ cell neoplasia: suppressed translation of mRNA in pre-invasive carcinoma in situ but increased protein levels in advanced tumours
Si B Sonne, Christina E Hoei-Hansen, John E Nielsen, et al.
Expert Reviews in Molecular Medicine
|
July 2, 2015
Detection of skewed X-chromosome inactivation in Fragile X syndrome and X chromosome aneuploidy using quantitative melt analysis
David E Godler, Yoshimi Inaba, Charles E Schwartz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 13, 2012
Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study
Yoshimi Inaba, Amy S Herlihy, Charles E Schwartz, et al.
Page
of 1