Literature DB >> 1439769

The human Y chromosome: a 43-interval map based on naturally occurring deletions.

D Vollrath1, S Foote, A Hilton, L G Brown, P Beer-Romero, J S Bogan, D C Page.   

Abstract

A deletion map of the human Y chromosome was constructed by testing 96 individuals with partial Y chromosomes for the presence or absence of many DNA loci. The individuals studied included XX males, XY females, and persons in whom chromosome banding had revealed translocated, deleted, isodicentric, or ring Y chromosomes. Most of the 132 Y chromosomal loci mapped were sequence-tagged sites, detected by means of the polymerase chain reaction. These studies resolved the euchromatic region (short arm, centromere, and proximal long arm) of the Y chromosome into 43 ordered intervals, all defined by naturally occurring chromosomal breakpoints and averaging less than 800 kilobases in length. This deletion map should be useful in identifying Y chromosomal genes, in exploring the origin of chromosomal disorders, and in tracing the evolution of the Y chromosome.

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Year:  1992        PMID: 1439769     DOI: 10.1126/science.1439769

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  75 in total

1.  Y chromosome haplotypes reveal prehistorical migrations to the Himalayas.

Authors:  B Su; C Xiao; R Deka; M T Seielstad; D Kangwanpong; J Xiao; D Lu; P Underhill; L Cavalli-Sforza; R Chakraborty; L Jin
Journal:  Hum Genet       Date:  2000-12       Impact factor: 4.132

2.  Population genetic implications from sequence variation in four Y chromosome genes.

Authors:  P Shen; F Wang; P A Underhill; C Franco; W H Yang; A Roxas; R Sung; A A Lin; R W Hyman; D Vollrath; R W Davis; L L Cavalli-Sforza; P J Oefner
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-20       Impact factor: 11.205

3.  Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypes.

Authors:  M F Hammer; A J Redd; E T Wood; M R Bonner; H Jarjanazi; T Karafet; S Santachiara-Benerecetti; A Oppenheim; M A Jobling; T Jenkins; H Ostrer; B Bonne-Tamir
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-06       Impact factor: 11.205

4.  Two male patients with ring Y: definition of an interval in Yq contributing to Turner syndrome.

Authors:  M Tzancheva; R Kaneva; P Kumanov; G Williams; C Tyler-Smith
Journal:  J Med Genet       Date:  1999-07       Impact factor: 6.318

5.  A molecular and FISH analysis of structurally abnormal Y chromosomes in patients with Turner syndrome.

Authors:  D O Robinson; P Dalton; P A Jacobs; K Mosse; M M Power; D H Skuse; J A Crolla
Journal:  J Med Genet       Date:  1999-04       Impact factor: 6.318

Review 6.  Gonadoblastoma, testicular and prostate cancers, and the TSPY gene.

Authors:  Y F Lau
Journal:  Am J Hum Genet       Date:  1999-04       Impact factor: 11.025

7.  Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome.

Authors:  K Kusz; M Kotecki; A Wojda; M Szarras-Czapnik; A Latos-Bielenska; A Warenik-Szymankiewicz; A Ruszczynska-Wolska; J Jaruzelska
Journal:  J Med Genet       Date:  1999-06       Impact factor: 6.318

8.  FISH deletion mapping defines a single location for the Y chromosome stature gene, GCY.

Authors:  S Kirsch; B Weiss; M De Rosa; T Ogata; G Lombardi; G A Rappold
Journal:  J Med Genet       Date:  2000-08       Impact factor: 6.318

9.  Multiplex PCR for screening of microdeletions on the Y chromosome.

Authors:  P Bor; J Hindkjaer; H J Ingerslev; S Kølvraa
Journal:  J Assist Reprod Genet       Date:  2001-05       Impact factor: 3.412

10.  TTY2: a multicopy Y-linked gene family.

Authors:  E Makrinou; M Fox; M Lovett; K Haworth; J M Cameron; K Taylor; Y H Edwards
Journal:  Genome Res       Date:  2001-06       Impact factor: 9.043

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