Publication:

Report of the committee on clinical disorders, chromosome aberrations and uniparental disomy

Date

Date

Date
1991
Journal Article
Published version

Citations

Citation copied

Frézal, J., Schinzel, A., & Neil, D. L. (1991). Report of the committee on clinical disorders, chromosome aberrations and uniparental disomy. Cytogenetic and Genome Research, 58(3–4), 986–1052. https://doi.org/10.1159/000133716

Abstract

Abstract

Abstract

There are more than 550 loci which have been associated with clinical disorders. Since HGM10.5, this number has been increased by 93 new entries belonging to all categories, from inborn errors of metabolism to congenital anomalies. In this report, we shall limit ourselves to hereditary diseases and congenital disorders and mention some constitutional liabilities to common diseases. We only list the references pertinent to the clinical disorders associated with mapped genes and not those relating to their assignment. Furthermore, we do

Additional indexing

Creators (Authors)

  • Frézal, J
  • Schinzel, Albert
  • Neil, D L

Journal/Series Title

Journal/Series Title

Journal/Series Title

Volume

Volume

Volume
58

Number

Number

Number
3-4

Page range/Item number

Page range/Item number

Page range/Item number
986

Page end

Page end

Page end
1052

Item Type

Item Type

Item Type
Journal Article

Dewey Decimal Classifikation

Dewey Decimal Classifikation

Dewey Decimal Classifikation

Keywords

Genetics (clinical), Genetics, Molecular Biology, uniparental disomy

Language

Language

Language
English

Publication date

Publication date

Publication date
1991-01-01

Date available

Date available

Date available
2023-09-27

Publisher

Publisher

Publisher

ISSN or e-ISSN

ISSN or e-ISSN

ISSN or e-ISSN
1424-8581

OA Status

OA Status

OA Status
Closed

PubMed ID

PubMed ID

PubMed ID

Other Identification Number

Other Identification Number

Other Identification Number
Corpus ID: 85031217

Citations

Citation copied

Frézal, J., Schinzel, A., & Neil, D. L. (1991). Report of the committee on clinical disorders, chromosome aberrations and uniparental disomy. Cytogenetic and Genome Research, 58(3–4), 986–1052. https://doi.org/10.1159/000133716

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Files
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