Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP

M. Simon; M. Phillips; H. Green; H. Stroh; K. Glatt; G. Bruns; S. A. Latt

Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP

M. Simon
, M. Phillips
, H. Green
, H. Stroh
, K. Glatt
, G. Bruns
, S. A. Latt

Oral Biology and Pathology

Harvard University

Research output: Contribution to journal › Article › peer-review

26 Scopus citations

Abstract

The human involucrin gene has been mapped to the region q21-q22 of chromosome 1. Three of six Utah families examined were polymorphic for a PstI fragment of the involucrin gene. In one individual, the variant PstI fragment was found by DNA sequencing to be missing one of the 39 repeats that make up two-thirds of the coding region.

Original language	English
Pages (from-to)	910-916
Number of pages	7
Journal	American Journal of Human Genetics
Volume	45
Issue number	6
State	Published - 1989

Cite this

@article{74fcc7c9f01b44368fe2835830d3f418,

title = "Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP",

abstract = "The human involucrin gene has been mapped to the region q21-q22 of chromosome 1. Three of six Utah families examined were polymorphic for a PstI fragment of the involucrin gene. In one individual, the variant PstI fragment was found by DNA sequencing to be missing one of the 39 repeats that make up two-thirds of the coding region.",

author = "M. Simon and M. Phillips and H. Green and H. Stroh and K. Glatt and G. Bruns and Latt, \{S. A.\}",

year = "1989",

language = "English",

volume = "45",

pages = "910--916",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

number = "6",

}

TY - JOUR

T1 - Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP

AU - Simon, M.

AU - Phillips, M.

AU - Green, H.

AU - Stroh, H.

AU - Glatt, K.

AU - Bruns, G.

AU - Latt, S. A.

PY - 1989

Y1 - 1989

N2 - The human involucrin gene has been mapped to the region q21-q22 of chromosome 1. Three of six Utah families examined were polymorphic for a PstI fragment of the involucrin gene. In one individual, the variant PstI fragment was found by DNA sequencing to be missing one of the 39 repeats that make up two-thirds of the coding region.

AB - The human involucrin gene has been mapped to the region q21-q22 of chromosome 1. Three of six Utah families examined were polymorphic for a PstI fragment of the involucrin gene. In one individual, the variant PstI fragment was found by DNA sequencing to be missing one of the 39 repeats that make up two-thirds of the coding region.

UR - https://www.scopus.com/pages/publications/0024827189

M3 - Article

C2 - 2574003

AN - SCOPUS:0024827189

SN - 0002-9297

VL - 45

SP - 910

EP - 916

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 6

ER -

Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP

Abstract

Other files and links

Fingerprint

Cite this