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Ruth McGowan

Showing results (11-20 of 44) with videos related to

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BMJ Open|April 4, 2020
Birth incidence, deaths and hospitalisations of children and young people with Down syndrome, 1990-2015: birth cohort studyLaura Anne Hughes-McCormack, Ruth McGowan, J P Pell, et al.
Clinical Endocrinology|November 21, 2025
The Use of Routine Laboratory 17-Hydroxyprogesterone for Identification of Cases of 21-Hydroxylase Deficiency Congenital Adrenal HyperplasiaJoseph McElvaney, Salma R Ali, Amy R Frank, et al.
Clinical Genetics|March 21, 2012
Results of Duchenne muscular dystrophy family screening in practice: leaks rather than cascades?Ruth McGowan, Benjamin R Challoner, Sarah Ross, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|May 31, 2022
The Use of Genetics for Reaching a Diagnosis in XY DSDS Faisal Ahmed, Malika Alimusina, Rafael L Batista, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|January 15, 2016
The outcome of prenatal identification of sex chromosome abnormalitiesAngela K Lucas-Herald, Fiona Cann, Lorna Crawford, et al.
Journal of Clinical Research in Pediatric Endocrinology|March 20, 2018
Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of LifeFiliz Mine Çizmecioğlu, Jeremy Huw Jones, Wendy Forsyth Paterson, et al.
Hormone Research in Paediatrics|November 27, 2023
Thioredoxin Reductase 2 Variant as a Cause of Micropenis, Undescended Testis, and Selective Glucocorticoid DeficiencySupitcha Patjamontri, Angela K Lucas-Herald, Martin McMillan, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutationsJoanna McCauley, Navta Masand, Ruth McGowan, et al.
The Journal of Clinical Endocrinology and Metabolism|February 5, 2020
Serum Anti-Müllerian Hormone in the Prediction of Response to hCG Stimulation in Children With DSDAngela K Lucas-Herald, Andreas Kyriakou, Malika Alimussina, et al.
Fertility and Sterility|February 25, 2015
DNA copy number variations are important in the complex genetic architecture of müllerian disordersRuth McGowan, Graham Tydeman, David Shapiro, et al.
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
BMJ Open|April 4, 2020
Birth incidence, deaths and hospitalisations of children and young people with Down syndrome, 1990-2015: birth cohort studyLaura Anne Hughes-McCormack, Ruth McGowan, J P Pell, et al.
Clinical Endocrinology|November 21, 2025
The Use of Routine Laboratory 17-Hydroxyprogesterone for Identification of Cases of 21-Hydroxylase Deficiency Congenital Adrenal HyperplasiaJoseph McElvaney, Salma R Ali, Amy R Frank, et al.
Clinical Genetics|March 21, 2012
Results of Duchenne muscular dystrophy family screening in practice: leaks rather than cascades?Ruth McGowan, Benjamin R Challoner, Sarah Ross, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|May 31, 2022
The Use of Genetics for Reaching a Diagnosis in XY DSDS Faisal Ahmed, Malika Alimusina, Rafael L Batista, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|January 15, 2016
The outcome of prenatal identification of sex chromosome abnormalitiesAngela K Lucas-Herald, Fiona Cann, Lorna Crawford, et al.
Journal of Clinical Research in Pediatric Endocrinology|March 20, 2018
Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of LifeFiliz Mine Çizmecioğlu, Jeremy Huw Jones, Wendy Forsyth Paterson, et al.
Hormone Research in Paediatrics|November 27, 2023
Thioredoxin Reductase 2 Variant as a Cause of Micropenis, Undescended Testis, and Selective Glucocorticoid DeficiencySupitcha Patjamontri, Angela K Lucas-Herald, Martin McMillan, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutationsJoanna McCauley, Navta Masand, Ruth McGowan, et al.
The Journal of Clinical Endocrinology and Metabolism|February 5, 2020
Serum Anti-Müllerian Hormone in the Prediction of Response to hCG Stimulation in Children With DSDAngela K Lucas-Herald, Andreas Kyriakou, Malika Alimussina, et al.
Fertility and Sterility|February 25, 2015
DNA copy number variations are important in the complex genetic architecture of müllerian disordersRuth McGowan, Graham Tydeman, David Shapiro, et al.
Pageof 5