Background: Array CGH is a powerful tool for the detection of copy number changes in the genome. Methods: We have developed a human X and Y chromosome tiling path array for the analysis of sex chromosome aberrations. Results: Normal X and Y chromosome profiles were established by analysis with DNA from normal fertile male and female individuals. Infertile males with known Y deletions confirmed the competence of the array to detect AZFa, AZFb and AZFc deletions and to distinguish between different AZFc lesions. Examples of terminal and interstitial deletions of Xp (previously characterised through cytogenetic and microsatellite analysis - [Lachlan et al, 2006]) have been assessed on the arrays both confirming and refining the established deletion breakpoints. Breakpoints in iso-Yq, iso-Yp and X-Y translocation chromosomes and X-Y interchanges in XX males are also amenable to analysis. Discussion: The resolution of the tiling path clone set used allows breakpoints to be placed within 100-200Kb, ...
Triple X syndrome, also known as trisomy X and 47,XXX, is characterized by the presence of an extra X chromosome in each cell of a female.[1] Those affected are often taller than average.[1] Usually there are no other physical differences and normal fertility.[1] Occasionally there are learning difficulties, decreased muscle tone, seizures, or kidney problems.[1] Triple X is due to a random event.[1] Triple X can result either during the division of the mothers reproductive cells or during division of cells during early development.[2] It is not typically inherited from one generation to the next.[1] A form where only a percentage of the body cells contain XXX can also occur.[1] Diagnosis is by chromosomal analysis.[3] Treatment may include speech therapy, physical therapy, and counseling.[3] It occurs in about one in every 1,000 female births.[2] It is estimated that 90% of those affected are not diagnosed as they either have no or only few symptoms.[2] It was first identified in 1959.[4] ...
Semantic Scholar extracted view of Environment and developmental risk in children with sex chromosome abnormalities. by Bruce G. Bender et al.
Triple X syndrome (also known as XXX syndrome, 47,XXX, and trisomy X) is a genetic condition found in girls only. Girls who have it may be taller than average, but the symptoms can vary greatly.
Free, official coding info for 2018 ICD-10-CM Q97.9 - includes detailed rules, notes, synonyms, ICD-9-CM conversion, index and annotation crosswalks, DRG grouping and more.
The gender taxonomy is a classification of the range of different levels at which humans vary in sexual characteristics. It is mainly used by medical specialists working in the area of sex research. John Money and Milton Diamond are probably the best known researchers in this field. Money earned his PhD for research into human hermaphroditism and pseudohermaphroditism, now known as intersex conditions. The taxonomy starts at the simplest, biological level and traces differentiations expressed at the increasingly complicated levels produced over the course of the human life cycle. Chromosomes (46,XX; 46,XY; 47,XXY ("Klinefelters syndrome"); 45,X0 ("Turner syndrome"); 47,XYY; 47,XXX ("Triple X syndrome"); XXXX syndrome; XXXXX syndrome, 48,XXYY syndrome, 46,XX/XY mosaic, other mosaic, and others) Gonads (testes, ovaries, one of each, ovotestes, other types of gonadal dysgenesis) Hormones (androgens: including testosterone; estrogens, including estradiol, estriol, estrone; antiandrogens and others) ...
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library(MASS) survey ,- na.omit(survey) head(survey) x ,- survey[, c(Sex, Wr.Hnd, NW.Hnd, Pulse)] names(x) ,- c(gender, iv1, iv2, dv) x$scaled_iv1 ,- scale(x$iv1, scale=FALSE) x$scaled_iv2 ,- scale(x$iv2, scale=FALSE) x$female_scaled_iv1 ,- scale(x$iv1, center=mean(x[x$gender == "Female", iv1]), scale=FALSE) x$female_scaled_iv2 ,- scale(x$iv2, center=mean(x[x$gender == "Female", iv2]), scale=FALSE) x$male_scaled_iv1 ,- scale(x$iv1, center=mean(x[x$gender == "Male", iv1]), scale=FALSE) x$male_scaled_iv2 ,- scale(x$iv2, center=mean(x[x$gender == "Male", iv2]), scale=FALSE) compare_fits ,- function(x) { fit1 ,- lm(dv ~ iv1+iv2, x) fit2 ,- lm(dv ~ iv1*iv2, x) fit3 ,- lm(dv ~ scaled_iv1*scaled_iv2, x) fit4 ,- lm(dv ~ male_scaled_iv1*male_scaled_iv2, x) fit5 ,- lm(dv ~ female_scaled_iv1*female_scaled_iv2, x) results ,- list() results$p_normal ,- anova(fit1, fit2)[2,6] results$p_centered ,- anova(fit1, fit3)[2,6] results$p_centered_male ,- anova(fit1, fit4)[2,6] ...
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... Qla4xxx can just call the iscsi recovery functions directly. There is no need for userspace to do this for qla4xxx, because we do not use the mutex to iterate over devices anymore and iscsi_block /unblock_session can be called from interrupt context or the dpc thread. And having userspace do this just creates uneeded headaches for qla4xxx root situations where the session may experience problems. For example during the kernel shutdown the scsi layer wants to send sync caches, but at this time userspace is not up (iscsid is not running), so we cannot recover from the problem. Signed-off-by: Mike Christie ,[EMAIL PROTECTED], Cc: David Somayajulu ,[EMAIL PROTECTED], Signed-off-by: James Bottomley ,[EMAIL PROTECTED], --- drivers/scsi/qla4xxx/ql4_init.c , 1 + drivers/scsi/qla4xxx/ql4_os.c , 40 +++----------------------------------- 2 files changed, 5 insertions(+), 36 deletions(-) diff --git a/drivers/scsi/qla4xxx/ql4_init.c ...
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export ftp_proxy=http://xxx.xxx.xxx.xxx:yy , e export http_proxy=http://xxx.xxx.xxx.xxx:yy;. Só troca os xs pelo ip e os ys pela porta. Rnaldo On Tue, 2003-07-08 at 15:16, Sergio wrote: , Pessoal, , , Como faco a configuracao do proxy no modo texto? , , Estou em Internet Predial, que possui proxy. Pelo navegador configurei o , proxy e navego. Mas nao consigo fazer o apt-get update porque o modo , texto está fora do ar. , , Sergio , , , , , -- , To UNSUBSCRIBE, email to [email protected] , with a subject of unsubscribe. Trouble? Contact [email protected] ...
On Thu, Jun 11, 2009 at 2:19 PM, Wolfgang Denk,[email protected], wrote: , So far, MPC512x used mpc512x_find_ips_freq() to get the bus frequency, , while MPC52xx used mpc52xx_find_ipb_freq(). Despite the different , clock names (IPS vs. IPB) the code was identical. , , Use common code for both processor families. , , Signed-off-by: Wolfgang Denk ,[email protected], , Cc: Grant Likely ,[email protected], , Cc: Kumar Gala ,[email protected], You probably already know this, but this patch doesnt apply against mainline, so I wont merge for 2.6.31. g. , --- , , This patch is not only intended to avoid code duplication, but it , will be needed in a following patch that fixes a MII speed , miscalculation in drivers/net/fs_enet/mii-fec.c - this patch allows , for a clean solution that works both on MPC512x and MPC52x systems. , , arch/powerpc/include/asm/mpc512x.h , 22 ----------------- , arch/powerpc/include/asm/mpc52xx.h , 2 +- , arch/powerpc/include/asm/mpc5xxx.h , 22 +++++++++++++++++ , ...
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progn (setq xxx 1) , (goto-char 1) , (insert x) , (setq o (make-overlay 1 2)) , (overlay-put o modification-hooks (list (lambda (ov dummy b e , &optional l) , (setq xxx 0)))) , (overlay-put o evaporate t) , (delete-char 1) , xxx) And the above code only tests whether `modification-hooks works, not whether `evaporate works. As for my initial remark about `evaporate working, I meant Im not sure if it does what we want here when I said Im not sure itll work. I know `evaporate does work in the sense that it does what its documented to do (otherwise Id have fixed it or filed a bug report). Stefan ...
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程序实现下面提供了部分代码的节选。 1.提供JMXWebLogicHelper作为获取连接的工具。 public class JMXWebLogicHelper implements JMXHelper { /** * 获取JMXMBeanServer连接 * * @param URI * Consts.URI_XXX * @param protocol * 协议 weblogic为T3 * @param hostname * 主机IP地址 * @param port * 端口
Abstract. Primary amenorrhea which result commonly from sex chromosome aberration as geneticabnormalities, may result from oneaberration in autosomal chromosomes or in association with sex chromosomal aberrations. Chromosomal analysis was performed for the 26 years old lady (married and infertile) with primary amenorrhea by using G-band technique. Four autosomal chromosomes are involved in producing primary amenorrhea with normal phenotype, secondary characteristics were associated with mosaic karyotypes the1st: 46,XX,(3;5;10)(q13-23;q23-35;22-25),(5;19)(qter;p13.2),del(19p13.2).2nd: 45,XX, ,(3;5;10)(q13-23;q23-35;22-25),del(12),del(12),del(19p13.2),(M).The sex chromosomes look normal.The conclusion was that may be some autosomal chromosomes regulate reproductive development and may the alerted regions on chromosomes in recent study have effect somehow on regulation of reproductive development.. انقطاع الطمث الابتدائي الذي يمثل احد التشوهات الجنينية ...
TY - JOUR. T1 - Heterozygous fragile X female. T2 - Historical, physical, cognitive, and cytogenetic features. AU - Cronister, A.. AU - Schreiner, R.. AU - Wittenberger, M.. AU - Amiri, K.. AU - Harris, K.. AU - Hagerman, Randi J. PY - 1991. Y1 - 1991. N2 - Historical, physical, cognitive, and cytogenetic data were documented in 105 heterozygous fragile X [fra(X)] females and 90 controls in a prospective fashion. For comparisons, we divided heterozygotes and controls into those with cognitive impairment (IQ , 85) and normal IQ (IQ ≥ 85). The only finding that was significantly more frequent in impaired heterozygotes compared with impaired controls χ2 analysis was shyness. Features that were more frequent in normal IQ heterozygotes compared with normal controls were voluntary thumb dislocation and hyperextensible metacarpal-phalangeal (MP) joints. Comparisons among heterozygotes demonstrated more math problems, hand biting, strabismus, high-arched palate, hyperextensible finger joints, and ...
Free, official coding info for 2020 ICD-10-CM Q98.7 - includes detailed rules, notes, synonyms, ICD-9-CM conversion, index and annotation crosswalks, DRG grouping and more.
TY - JOUR. T1 - CT and ultrasound features of metanephric adenoma in adults with pathologic correlation. AU - Fielding, Julia R.. AU - Visweswaran, Aparna. AU - Silverman, Stuart G.. AU - Granter, Scott R.. AU - Renshaw, Andrew A.. PY - 1999/5/1. Y1 - 1999/5/1. N2 - Purpose: The purpose of this work was to correlate the CT, ultrasound, and pathologic features of metanephric adenoma, a rare benign renal tumor in adults. Method: Retrospective review of medical records (1990-1997) revealed three adult female patients who had both preoperative imaging and nephrectomy with pathologic diagnosis of metanephric adenoma performed at our institution. CT (n = 3) and ultrasound (n = 2) features were reviewed in consensus by two radiologists and correlated with pathologic findings. Results: In all three cases, the metanephric adenoma was of increased attenuation relative to adjacent renal parenchyma on unenhanced CT scans. No septa or calcifications were seen. Ultrasound images showed both tumors to be ...
How to Diagnose Turner Syndrome. Turner Syndrome (TS) is a relatively rare condition that affects only females and is caused by a sex chromosome abnormality. It can cause a wide range of physical and developmental challenges, but early...
Turners syndrome, one of the most common sex chromosome abnormalities in females, is caused by loss of part or all of an X chromosome. We report a case of mosaic Turners syndrome, posted for elective cesarean delivery under low-dose sequential combined spinal epidural anesthesia. The unique features of this case were the combination of an anticipated difficult airway and both short stature and scoliosis in the lumbar region. A titrated combined spinal-epidural technique was performed in order to avoid hemodynamic instability, which could have been exacerbated in the presence of cardiovascular deformities that accompany this syndrome in many cases ...
PGD has become a relatively recent indication for IVF. PGD allows diagnosis at three levels: sex chromosome abnormalities/aneuploidy, structural chromosomal abnormalities, and single-gene diagnosis. The first reported cases of PGD were undertaken for sex determination of embryos to prevent transmission of X-linked genetic disorders. These initial cases were reported in 1989. Subsequently, PGD was used to prevent single-gene disorders such as cystic fibrosis. The two most common single-gene disorders diagnosed by PGD are cystic fibrosis and sickle cell disease.97 Recently, the indications for PGD have been expanded to include the diagnosis of embryo aneuploidy in women of advanced maternal age, previous IVF failures, and history of previously affected embryos or offspring. Diagnosis of structural chromosomal abnormalities in couples with balanced translocations is also possible with PGD, particularly in the treatment of recurrent miscarriage. Recently, whole-genome amplification with comparative ...
Semantic Scholar extracted view of Three unusual trisomic patterns in children. Triple X plus triple E-triple X mosaic: normal XY-D trisomy mosaic; partial trisomy with E translocation. by Emerson Engel et al.
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Synonyms for sex-chromosome at Thesaurus.com with free online thesaurus, antonyms, and definitions. Dictionary and Word of the Day.
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II. Using tra-1 mutations. tra-1(o) mutations [(o) signifies a loss of gene function] are recessive and turn the animals (whether XO or XX) into phenotypic males.. tra-1(d) mutations are dominant and turn XO or XX animals into females.. The tra-1 gene is on the third chromosome.. The cross tra-1(d)/tra-1(o)female X tra-1(o)/tra-1(o)male will produce the same male and female progeny.. If we rename the tra-1(d)-containing chromosome W and the tra-1(o)-containing chromosome Z, we see that we have a WZ/ZZ system.. ...
Objective: To study the clinical characteristics, image findings, therapeutic method and prognosis of metanephric adenoma. Method: The clinical characteristic, image findings, operation methods and prognosis of 16 metanephric adenoma patients treated at Department of Urology, Peking University First Hospital from January 2004 to March 2016 were analyzed retrospectively. Results: There were 6 male and 10 female patients in the study. The mean age of patients was 33.7 years (ranging from 14 to 83 years). Two patients came to the hospital because of fever, while other 14 patients had no symptoms and found renal tumor by medical examination ...
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