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Also searching for:Chromosome 6via MeSH
Showing 110 of 10 results for Chromosomes, Human, Pair 6

2 New Developments in LGBT Development: What’s New and What’s (Still) True

6), 585–597. doi:10.1007/s10566-013-9219-9 Forssell, S. L., Gamache, P., & Dwan, R. (2017). Approaches to interventions with LGBT populations. Manuscript in preparation, Department of Psychology, The George Washington University, Washington, DC, 65. Fox, J., & Ralston, R. (2016). Queer identity online: Informal learning and teaching experiences of LGBTQ individuals
Richard Ruth and Erik Santacruz· WILEY· 9988778899889Book detail →

2 New Developments in LGBT Development: What’s New and What’s (Still) True

6), 585–597. doi:10.1007/s10566-013-9219-9 Forssell, S. L., Gamache, P., & Dwan, R. (2017). Approaches to interventions with LGBT populations. Manuscript in preparation, Department of Psychology, The George Washington University, Washington, DC, 65. Fox, J., & Ralston, R. (2016). Queer identity online: Informal learning and teaching experiences of LGBTQ individuals
Richard Ruth and Erik Santacruz· Oxford· 9988998899889Book detail →

9 Health Disparities and LGBT Populations

chromosomal, gonadal, or anatomic) who have been subject to a medical system that enacted societal stigmatization of DSD (Eckstrand & Sciolla, 2014). The results included the medical profession subjecting children diagnosed with DSD to “highly invasive and sometimes damaging interventions” to “ensure sex and gender normalization” (Eckstrand & Sciolla
Richard Ruth and Erik Santacruz· WILEY· 9988778899889Book detail →

9 Health Disparities and LGBT Populations

chromosomal, gonadal, or anatomic) who have been subject to a medical system that enacted societal stigmatization of DSD (Eckstrand & Sciolla, 2014). The results included the medical profession subjecting children diagnosed with DSD to “highly invasive and sometimes damaging interventions” to “ensure sex and gender normalization” (Eckstrand & Sciolla
Richard Ruth and Erik Santacruz· Oxford· 9988998899889Book detail →

Foreword

chromosomes and every person a gender as that person’s self-representation as male, female, or nonbinary. Arthritis is a leading cause of disability and medical healthcare expenditure in the United States. The burden of knee osteoarthritis is strikingly greater for females,2 yet our understanding of this disparity
Claudette M. Lajam· Oxford· 7766778899887Book detail →
Pediatric Neurology · Chapter 100

Case 77 Tell Me How You Eat and I Will Tell You How You Walk

6–10 mg/dl). Genetic testing showed two com­pound heterozygous pathogenic variants in the TTPA gene, leading to a loss of α‐TTP activity. The variants identified were c.661C>T (p.Arg221Trp) and c.744delA (p.Glu249Asnfster15). The child was put on high doses (1000 mg/day) of oral vitamin E. Clinical Differential Diagnoses
Hugo A. Arroyo· Elsevier Inc.· 9123456780105Book detail →
Pediatric Neurology · Chapter 100

Case 77 Tell Me How You Eat and I Will Tell You How You Walk

6–10 mg/dl). Genetic testing showed two com­pound heterozygous pathogenic variants in the TTPA gene, leading to a loss of α‐TTP activity. The variants identified were c.661C>T (p.Arg221Trp) and c.744delA (p.Glu249Asnfster15). The child was put on high doses (1000 mg/day) of oral vitamin E. Clinical Differential Diagnoses
Hugo A. Arroyo· Elsevier Inc.· 9123456798765Book detail →
Pediatric Neurology · Chapter 100

Case 77 Tell Me How You Eat and I Will Tell You How You Walk

6–10 mg/dl). Genetic testing showed two com­pound heterozygous pathogenic variants in the TTPA gene, leading to a loss of α‐TTP activity. The variants identified were c.661C>T (p.Arg221Trp) and c.744delA (p.Glu249Asnfster15). The child was put on high doses (1000 mg/day) of oral vitamin E. Clinical Differential Diagnoses
Hugo A. Arroyo· Elsevier Inc.· 8363524232526Book detail →

4.  Autoimmune disorders

6-16. 20. Amur S, Parekh A & Mummaneni P. Sex differences and genomics in autoimmune diseases J Autoimmun 2-3, 2012;38: J254-J265. 21. Ozcelik T. X chromosome
Claudette M. Lajam· Oxford· 7766778899887Book detail →

5.  Arthroplasty in the hypermobile patient

chromosome 21, which encodes the genes for type VI collagen.14 OI and EDS also affect collagen, either via mutations to the genes encoding collagen itself or via mutation to the genes encoding enzymes involved in posttranslational modification of collagen.15,16 OI affects type I collagen—the major type
Claudette M. Lajam· Oxford· 7766778899887Book detail →
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