(Q41341329)

29 September 2017

1 reference

title

Dominance and homozygosity (English)

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29 September 2017

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J Zlotogora

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29 September 2017

publication date

1 February 1997

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American Journal of Medical Genetics Part A

29 September 2017

published in

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29 September 2017

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29 September 2017

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29 September 2017

page(s)

412-416

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A large Turkish kindred with syndactyly type II (synpolydactyly). 2. Homozygous phenotype?

29 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970211%2968%3A4%3C412%3A%3AAID-AJMG8%3E3.0.CO%3B2-N

PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970211%2968%3A4%3C412%3A%3AAID-AJMG8%3E3.0.CO%3B2-N

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970211%2968%3A4%3C412%3A%3AAID-AJMG8%3E3.0.CO%3B2-N

Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970211%2968%3A4%3C412%3A%3AAID-AJMG8%3E3.0.CO%3B2-N

Charcot-Marie-Tooth disease: a new paradigm for the mechanism of inherited disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970211%2968%3A4%3C412%3A%3AAID-AJMG8%3E3.0.CO%3B2-N

Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970211%2968%3A4%3C412%3A%3AAID-AJMG8%3E3.0.CO%3B2-N

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970211%2968%3A4%3C412%3A%3AAID-AJMG8%3E3.0.CO%3B2-N

The mutational spectrum in Waardenburg syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970211%2968%3A4%3C412%3A%3AAID-AJMG8%3E3.0.CO%3B2-N

Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970211%2968%3A4%3C412%3A%3AAID-AJMG8%3E3.0.CO%3B2-N

Homozygotes for Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970211%2968%3A4%3C412%3A%3AAID-AJMG8%3E3.0.CO%3B2-N

The molecular basis of genetic dominance

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970211%2968%3A4%3C412%3A%3AAID-AJMG8%3E3.0.CO%3B2-N

Molecular features of the CAG repeats and clinical manifestation of Machado--Joseph disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970211%2968%3A4%3C412%3A%3AAID-AJMG8%3E3.0.CO%3B2-N

How trinucleotide repeats may function

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970211%2968%3A4%3C412%3A%3AAID-AJMG8%3E3.0.CO%3B2-N

10.1002/(SICI)1096-8628(19970211)68:4<412::AID-AJMG8>3.0.CO;2-N

21 January 2018

Identifiers

DOI

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29 September 2017

1 reference