Non-fluorescent and non-heterochromatic Y chromosome in 45, X 46,XY mosaicism. 1974

L Y Hsu, and H J Kim, and S Paciuc, and L Steinfeld, and K HirshhorHirschhorn

UI MeSH Term Description Entries
D008297 Male Males
D009030 Mosaicism The occurrence in an individual of two or more cell populations of different chromosomal constitutions, derived from a single ZYGOTE, as opposed to CHIMERISM in which the different cell populations are derived from more than one zygote.
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D005453 Fluorescence The property of emitting radiation while being irradiated. The radiation emitted is usually of longer wavelength than that incident or absorbed, e.g., a substance can be irradiated with invisible radiation and emit visible light. X-ray fluorescence is used in diagnosis.
D006570 Heterochromatin The portion of chromosome material that remains condensed and is transcriptionally inactive during INTERPHASE. Heterochromatins
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D012730 Sex Chromosomes The homologous chromosomes that are dissimilar in the heterogametic sex. There are the X CHROMOSOME, the Y CHROMOSOME, and the W, Z chromosomes (in animals in which the female is the heterogametic sex (the silkworm moth Bombyx mori, for example)). In such cases the W chromosome is the female-determining and the male is ZZ. (From King & Stansfield, A Dictionary of Genetics, 4th ed) Gonosomes,Chromosome, Sex,Chromosomes, Sex,Gonosome,Sex Chromosome
D014424 Turner Syndrome A syndrome of defective gonadal development in phenotypic females associated with the karyotype 45,X (or 45,XO). Patients generally are of short stature with undifferentiated GONADS (streak gonads), SEXUAL INFANTILISM, HYPOGONADISM, webbing of the neck, cubitus valgus, elevated GONADOTROPINS, decreased ESTRADIOL level in blood, and CONGENITAL HEART DEFECTS. NOONAN SYNDROME (also called Pseudo-Turner Syndrome and Male Turner Syndrome) resembles this disorder; however, it occurs in males and females with a normal karyotype and is inherited as an autosomal dominant. Bonnevie-Ullrich Syndrome,Gonadal Dysgenesis, 45,X,Gonadal Dysgenesis, XO,Monosomy X,Status Bonnevie-Ullrich,Turner's Syndrome,Ullrich-Turner Syndrome,Bonnevie Ullrich Syndrome,Status Bonnevie Ullrich,Syndrome, Ullrich-Turner,Turners Syndrome,Ullrich Turner Syndrome,XO Gonadal Dysgenesis

Related Publications

L Y Hsu, and H J Kim, and S Paciuc, and L Steinfeld, and K HirshhorHirschhorn
April 1986, Archives francaises de pediatrie,
L Y Hsu, and H J Kim, and S Paciuc, and L Steinfeld, and K HirshhorHirschhorn
January 1980, Annales de genetique,
L Y Hsu, and H J Kim, and S Paciuc, and L Steinfeld, and K HirshhorHirschhorn
June 1972, Annales de genetique,
L Y Hsu, and H J Kim, and S Paciuc, and L Steinfeld, and K HirshhorHirschhorn
January 2001, Ryoikibetsu shokogun shirizu,
L Y Hsu, and H J Kim, and S Paciuc, and L Steinfeld, and K HirshhorHirschhorn
September 1978, Journal de genetique humaine,
L Y Hsu, and H J Kim, and S Paciuc, and L Steinfeld, and K HirshhorHirschhorn
February 2024, Zhonghua er ke za zhi = Chinese journal of pediatrics,
L Y Hsu, and H J Kim, and S Paciuc, and L Steinfeld, and K HirshhorHirschhorn
March 1978, Annales de genetique,
L Y Hsu, and H J Kim, and S Paciuc, and L Steinfeld, and K HirshhorHirschhorn
November 2017, Annals of clinical and laboratory science,
L Y Hsu, and H J Kim, and S Paciuc, and L Steinfeld, and K HirshhorHirschhorn
May 2006, American journal of medical genetics. Part A,
L Y Hsu, and H J Kim, and S Paciuc, and L Steinfeld, and K HirshhorHirschhorn
January 2020, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas,
Copied contents to your clipboard!