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*  Wild Sex in Zebrafish: Loss of the Natural Sex Determinant in Domesticated Strains | Genetics
2001 Meiotic chromosomes and stages of sex chromosome evolution in fish: zebrafish, platyfish and guppy. Chromosome Res. 9: 659 ... 2011 Effect of rearing temperatures during embryonic development on the phenotypic sex in zebrafish (Danio rerio). Sex Dev. 5: ... 2014 Zebrafish: a model vertebrate suitable for the analysis of human genetic disorders. Congenit. Anom. 54: 8-11. ... 2009 Sex determination and sex chromosome evolution: insights from medaka. Sex Dev. 3: 88-98. ...
  http://www.genetics.org/content/198/3/1291.full
*  FDNA and The Focus Foundation Join Forces to Help Children with Sex Chromosome Disorders Using Facia... ( ...
These d,FDNA,and,The,Focus,Foundation,Join,Forces,to,Help,Children,with,Sex,Chromosome,Disorders,Using,Facial,Analysis, ... PRWEB) May 10 2017 Millions of people worldwide are living with X and Y Chromosomal Disorders often called Sex Chromosome ... to accelerate the identification of people affected by X and Y Chromosomal Disorders. By training FDNA's facial analysis ... Millions of people worldwide are living with X and Y Chromosomal Disorders, often called Sex Chromosome Disorders, and don't ...
  http://www.bio-medicine.org/biology-technology-1/FDNA-and-The-Focus-Foundation-Join-Forces-to-Help-Children-with-Sex-Chromosome-Disorders-Using-Facial-Analysis-38318-1/
*  Melanie Manning | Stanford Medicine Profiles
Klinefelter syndrome is the most common sex chromosome disorder, affecting approximately 1/500 to 1/1000 males. The condition ... The chromosome 17q21.31 microdeletion syndrome is a novel genomic disorder that has originally been identified using high ... Fetal Alcohol Spectrum Disorders: Extending the Range of Structural Defects AMERICAN JOURNAL OF MEDICAL GENETICS PART A Jones, ... Severe liver disease in urea cycle disorders. Western Regional Meeting of the American-Federation-for-Medical-Research Traynor ...
  https://med.stanford.edu/profiles/melanie-manning
*  Most recent papers in the journal Case Reports in Ophthalmological Medicine | Read by QxMD
Turner syndrome is a common sex chromosome disorder affecting females. The disorder is caused by a partial loss, complete ... Therapeutic Effect of Anti-VEGF for Age-Related Macular Degeneration in the Untreated Fellow Eye. ... Results: Only the right eye was affected, and all examinations of the left eye were normal... ... agents have been reported to occasionally produce a therapeutic effect in the uninjected fellow eye. Here, three patients with ...
  https://www.readbyqxmd.com/journal/44011
*  Next Generation Sequencing expression profiling of mitochondrial subunits in men with Klinefelter syndrome [Abstract]
Objectives: Klinefelter syndrome (KS) is one of the most common sex-chromosome disorders as it affects up to 1 in every 600- ... Men with KS carry one extra X chromosome and they usually present a 47,XXY karyotype, but less frequent variants have also been ... the most common respiratory chain defect in human disorders. Since it has been shown that decreased Complex I protein levels ...
  http://www.medsci.org/v15p0031
*  Next Generation Sequencing expression profiling of mitochondrial subunits in men with Klinefelter syndrome
... is one of the most common sex-chromosome disorders. Men affected by KS carry one or more extra X-chromosome and the classic ... et al.Increased number of sex chromosomes affects height in a nonlinear fashion. a study of 305 patients with sex chromosome ... Objectives: Klinefelter syndrome (KS) is one of the most common sex-chromosome disorders as it affects up to 1 in every 600- ... of mtDNA of patients affected by the disorder [20]. Of notice, the polymorphisms found in the KS affected population were rare ...
  http://www.medsci.org/v15p0031.htm
*  Medical Home Portal - XXY (Klinefelter) Syndrome
Klinefelter Syndrome is caused by an extra X chromosome and affects development. Find information and resources to aid in ... XXY syndrome is the most common disorder of sex chromosomes, affecting approximately 1/1,000 males. [Morris: 2008] Variants are ... metabolic disorders such as homocystinuria, and overgrowth disorders such as Sotos syndrome. If routine chromosome studies are ... They can be differentiated definitively by genetic testing, which will demonstrate sex chromosome aneuploidy in individuals ...
  https://www.medicalhomeportal.org/diagnoses-and-conditions/xxy-syndrome
*  Hypertrichosis - Wikipedia
This form is an autosomal dominant (not located on the sex chromosomes) cutaneous disorder, that affects the skin. Generalized ... The affected son was named Maong-Phoset. He had an affected daughter named Mah-Me. Whereas all affected members of the family ... This condition may also be due to the change in the chromosome affecting the transcription of genes. Other hypertrichosis ... An affected female (carrying the hypertrichosis gene) has a 50% chance of passing it to her offspring. An affected male will ...
  https://en.wikipedia.org/wiki/Hypertrichosis
*  A Klinefelter boy with congenital adrenal hyperplasia: too much or too little androgens? | Springer for Research & Development
KS affects 1 in 667 live male births and is the most common sex chromosome disorder. It is the clinical result of an additional ... Cytogenetic and molecular study showed the presence of a marker chromosome, uniparental isodisomy of chromosome 6, and two ... Anti-Müllerian hormone and its clinical use in pediatrics with special emphasis on disorders of sex development. Int J ... he inherited the paternal chromosome carrying the point mutation A/CG intron 2 (655) and the maternal chromosome with the point ...
  https://rd.springer.com/article/10.1186/s13052-018-0485-x
*  Most recent papers with the keyword Verbal learning | Read by QxMD
Objectives: Klinefelter syndrome (KS) is one of the most common sex-chromosome disorders as it affects up to 1 in every 600- ... BACKGROUND: Bipolar disorder (BD) has been associated with dysfunctional resting-state brain functioning. However, it is still ... Men with KS carry one extra X chromosome and they usually present a 47,XXY karyotype, but less frequent variants have also been ... Resting-state fMRI signals in offspring of parents with bipolar disorder at the high-risk and ultra-high-risk stages and their ...
  https://www.readbyqxmd.com/keyword/15640
*  Developing a New Tool to Detect a Frequently Missed Sex Chromosome Disorder in Boys - Healthcanal.com : Healthcanal.com
Although infertility is the most frequent outcome of the disorder, affected individuals are also at high risk for ... and misunderstanding about the nature of sex chromosome disorders. "The physical features of the disorder are not well known, ... Home Mental Health and Behavior Developing a New Tool to Detect a Frequently Missed Sex Chromosome Disorder in Boys ... Developing a New Tool to Detect a Frequently Missed Sex Chromosome Disorder in Boys. ...
  https://www.healthcanal.com/mental-health-behavior/66426-developing-a-new-tool-to-detect-a-frequently-missed-sex-chromosome-disorder-in-boys.html
*  PPT - TURNER SYNDROME PowerPoint Presentation - ID:200179
Affects only females. Symptoms. Clinical features. Short stature (143-145cm tall)... ... What is Turner Syndrome?. Relatively common disorder caused by the loss of genetic material from one of the sex chromosomes. ... Relatively common disorder caused by the loss of genetic material from one of the sex chromosomes. Affects only females. ... Relatively common disorder caused by the loss of genetic material from one of the sex chromosomes. ...
  https://www.slideserve.com/Lucy/turner-syndrome
*  Dysplasias in Chromosome Disorders | Springer for Research & Development
... which affect all body cells, are generally more severe than those of the sex chromosomes. Rather massive anomalies in the ... are generally more severe than those of the sex chromosomes. Rather massive anomalies in the number of a sex chromosome, such ... Eggen, R. R.: Chromosome Diagnostics in Clinical Medicine. Springfield, Ill.: Ch. C Thomas 1965.Google Scholar ... Moreover, no whole chromosome anomalies have been observed for the larger autosomes (1-12), as these appear to be incompatible ...
  https://rd.springer.com/chapter/10.1007/978-3-7091-3338-5_33
*  Genetically Inherited Diseases: Gaucher's Disease
Genetic disorders are typically inherited (passed down) in either a dominant or recessive way. We each have two copies of every ... which means the disorder happens on a non-sex chromosome, affecting the metabolism, when a type of lipid called ... We each have two copies of every gene on our 22 numbered chromosomes. When a disorder is dominant, the disease can occur when ... When a disorder is recessive, there must be mistakes in both copies of the gene for the disorder to occur. This means that both ...
  https://www.ukessays.com/essays/biology/genetically-inherited-diseases-gauchers-1080.php
*  Human - Wikipedia
... some X and Y chromosome related conditions and disorders only affect either men or women. Other conditional differences between ... Like other mammals, humans have an XY sex-determination system, so that females have the sex chromosomes XX and males have XY.[ ... Among the 23 pairs of chromosomes there are 22 pairs of autosomes and one pair of sex chromosomes. ... chromosome 2 was formed from two other chromosomes, leaving humans with only 23 pairs of chromosomes, compared to 24 for the ...
  https://en.m.wikipedia.org/wiki/Human_being
*  Sex chromosome disorders - Wikipedia
Sex chromosome disorders belong to a group of genetic conditions that are caused or affected by the loss, damage or addition of ... sex chromosomes (gonosomes). In humans this may refer to: 45, X, also known as Turner syndrome 45,X/46,XY mosaicism 46, XX/XY ...
  https://en.wikipedia.org/wiki/Sex_chromosome_disorders
*  47 XXY | definition of 47 XXY by Medical dictionary
A male bodily disorder caused by one or more additional X (sex) chromosomes. Instead of the normal X and Y sex chromosomes, men ... The affected individuals are male (showing the SEX DETERMINATION role of the Y-chromosomes) but with much reduced fertility, ... associated with an abnormality of the sex chromosomes. It is associated typically with an XXY chromosome complement.. ... associated with an abnormality of the sex chromosomes. It is associated typically with an XXY chromosome complement. A similar ...
  http://medical-dictionary.thefreedictionary.com/47+XXY
*  VII - Genetic and Pediatric Diseases Flashcards by Mackie Mendoza | Brainscape
These disorders may result from alterations in the number or structure of chromosomes and may affect autosomes or sex ... These disorders may result from alterations in the number or structure of chromosomes and may affect autosomes or sex ... Autosomal dominant disorder. With this type, some patient do not have affected parents, has variations in penetrance and ... In X-linked disorders, female carriers are usually protected because of random inactivation of one X chromosome. ...
  https://www.brainscape.com/flashcards/vii-genetic-and-pediatric-diseases-3899594/packs/5734717
*  VII - Genetic and Pediatric Diseases Flashcards by Vince Luceno | Brainscape
These disorders may result from alterations in the number or structure of chromosomes and may affect autosomes or sex ... These disorders may result from alterations in the number or structure of chromosomes and may affect autosomes or sex ... An affected male does not transmit the disorder to sons but all daughters are carriers. ... This is a neurodegenerative genetic disorder that affects muscle coordination and leads to cognitive decline and psychiatric ...
  https://www.brainscape.com/flashcards/vii-genetic-and-pediatric-diseases-2399593/packs/4241965
*  Nat Turner Essay | Bartleby
... it is one of the most common sexual development disorders (Radtke et al. 2014). It is caused by an abnormal sex chromosome, ... Turner Thesis Summary Throughout history society has to go through many changes that not only affect many of the people but ... either an abnormal X chromosome or a missing X chromosome. The sex chromosome contributed by the father to the child determines ... sex of the child because the mother always contributes an X chromosome whereas the father can contribute either an X chromosome ...
  https://www.bartleby.com/topics/Nat-Turner-Essay
*  Von hippel lindau syndrome | Smore Newsletters
The X chromosome is affected by this disorder. Anyone can be affected by this disease. It is sex-linked because it is on the x ... What is VHL disorder? The von Hippel-Lindau syndrome is a disease that is an inherited disorder that characterizes the ...
  https://www.smore.com/wtzk1
*  Human Genetics
Examples of autosomal recessive disorders are albinism, cystic fibrosis.. X-linked genes are found on the sex X chromosome. X- ... Recessive X-linked disorders are rarely seen in females and usually only affect males. This is because males inherit their X ... The chromosomes are all numbered except for the X and the Y chromosomes, which are the sex chromosomes. In humans, as in all ... The chromosomes are all numbered except for the X and the Y chromosomes, which are the sex chromosomes. In humans, as in all ...
  https://www.euvolution.com/futurist-transhuman-news-blog/category/human-genetics
*  Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum...
... affected children (male-only, MO) or with at least one female, affected child (female-containing, FC). Loci showing evidence ... Large samples appear to yield more consistent results, and sex-stratified analyses facilitate the identification of sex- ... Suggestive sex-differential linkage was observed at 1p31.3 (MO), 8p21.2 (FC), and 8p12 (FC) in our discovery sample, and the MO ... No sex-differential signals met replication criteria, and no common SNPs were significantly associated with ASD within any ...
  https://molecularautism.biomedcentral.com/articles/10.1186/2040-2392-5-13
*  Cracks in the code: Why mapping your DNA may be less reliable than you think - The Globe and Mail
... the X sex chromosome, of which women usually have two copies. On paper, No. 27 has mosaic Turner syndrome, a rare disorder that ... "People are walking around with these massive chunks of chromosomes missing, and [duplications] that affect multiple genes," Dr ... researchers have generally hunted for disease mutations by looking at people who have a particular disorder, or affected family ... CHROMOSOME. They are comprised of one tightly coiled molecule of deoxyribonucleic acid (DNA) with proteins that serve to ...
  https://www.theglobeandmail.com/technology/science/genetic-testing/article37829424/