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Literature DB >> 881713

Xg groups and sex chromosome abnormalities in people of northern European ancestry: an addendum.

R Sanger, P Tippett, J Gavin, P Teesdale, G L Daniels.

Abstract

Entities: Disease Species

Mesh：

Substances：
Blood Group Antigens

Year: 1977 PMID： 881713 PMCID： PMC1013559 DOI： 10.1136/jmg.14.3.210

Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318

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7 in total

1. XX SEX CHROMOSOMES IN A HUMAN MALE. FIRST CASE.

Authors: A DELACHAPELLE; H HORTLING; M NIEMI; J WENNSTROEM
Journal: Acta Med Scand Date: 1964

2. Parental origin of the sex chromosomes in the XO and XXY karyotypes in man.

Authors: G R FRASER
Journal: Ann Hum Genet Date: 1963-06 Impact factor: 1.670

3. A sex-linked blood group.

Authors: J D MANN; A CAHAN; A G GELB; N FISHER; J HAMPER; P TIPPETT; R SANGER; R R RACE
Journal: Lancet Date: 1962-01-06 Impact factor: 79.321

4. X g and X chromosome inactivation.

Authors: J Ducos; Y Marty; R Sanger; R R Race
Journal: Lancet Date: 1971-07-24 Impact factor: 79.321

5. Xg groups and sex abnormalities in people of northern European ancestry.

Authors: R Sanger; P Tippett; J Gavin
Journal: J Med Genet Date: 1971-12 Impact factor: 6.318

6. The X-linked blood group system Xg. Tests on unrelated people and families of northern European ancestry.

Authors: R Sanger; P Tippett; J Gavin
Journal: J Med Genet Date: 1971-12 Impact factor: 6.318

7. Evidence that the Xg locus is inactivated in structurally abnormal X chromosomes.

Authors: P E Polani; R Angell; F Giannelli; A De la Chapelle; R R Race; R Sanger
Journal: Nature Date: 1970-08-08 Impact factor: 49.962

7 in total

19 in total

1. The parental origin of the single X chromosome in Turner syndrome: lack of correlation with parental age or clinical phenotype.

Authors: A Mathur; L Stekol; D Schatz; N K MacLaren; M L Scott; B Lippe
Journal: Am J Hum Genet Date: 1991-04 Impact factor: 11.025

2. A cytogenetic and molecular study of a series of 45,X fetuses and their parents.

Authors: A Cockwell; M MacKenzie; S Youings; P Jacobs
Journal: J Med Genet Date: 1991-03 Impact factor: 6.318

3. Coincident maternal meiotic nondisjunction of chromosomes X and 21 without evidence of autosomal asynapsis.

Authors: R S Ikonen; M Lindlöf; M O Janas; K O Simola; A Millington-Ward; A de la Chapelle
Journal: Hum Genet Date: 1989-10 Impact factor: 4.132

4. Determination of the parental origin of sex-chromosome monosomy using restriction fragment length polymorphisms.

Authors: T Hassold; E Kumlin; N Takaesu; M Leppert
Journal: Am J Hum Genet Date: 1985-09 Impact factor: 11.025

5. Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis.

Authors: A Rinaldi; N Archidiacono; M Rocchi; G Filippi
Journal: J Med Genet Date: 1979-06 Impact factor: 6.318