Craniofacial anthropometric analysis in several types of chondrodysplasia (Q71771333)

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21 October 2019

title

Craniofacial anthropometric analysis in several types of chondrodysplasia (English)

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21 October 2019

Hunter AG

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21 October 2019

publication date

1 October 1996

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American Journal of Medical Genetics Part A

21 October 2019

published in

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21 October 2019

volume

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21 October 2019

issue

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21 October 2019

page(s)

5-12

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Anthropometric craniofacial pattern profiles in Down syndrome

21 October 2019

cites work

1 reference

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A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia

21 January 2018

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Abnormal measurements and disproportions in the face of Down's syndrome patients: preliminary report of an anthropometric study

21 January 2018

1 reference

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The genetic entity of hypochondroplasia

21 January 2018

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Applications of pattern profile analysis to malformations of the head and face

21 January 2018

1 reference

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Hypochondroplasia: Clinical and Radiological Aspects in 39 cases

21 January 2018

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Follow-up study of patients with Wiedemann-Beckwith syndrome with emphasis on the change in facial appearance over time

21 January 2018

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A gene for achondroplasia–hypochondroplasia maps to chromosome 4p

21 January 2018

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Observations suggesting allelism of the achondroplasia and hypochondroplasia genes.

21 January 2018

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

21 January 2018

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A glycine 375-to-cysteine substitution in the transmembrane domain of the fibroblast growth factor receptor-3 in a newborn with achondroplasia

21 January 2018

1 reference

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Anthropometric analysis of the face in hypohidrotic ectodermal dysplasia: a family study

21 January 2018

1 reference

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10.1002/(SICI)1096-8628(19961002)65:1<5::AID-AJMG1>3.0.CO;2-U

21 January 2018

Identifiers

DOI

0 references

1 reference

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