Mirror hands and feet with a distinct nasal defect, an autosomal dominant condition-Reference-Cited by-同舟云学术

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Mirror hands and feet with a distinct nasal defect, an autosomal dominant condition

Published:1993-04-15 Issue:2 Volume:46 Page:129-131
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Martin Rick A.,Jones Marilyn C.,Jones Kenneth L.

Publisher

Wiley

Subject

Genetics (clinical)

Reference5 articles.

1. Ulnar dimelia

2. Mesomele Dysplasie: Falldarstellung und Literatur zum Werner-Syndrom

3. Hereditary Ulnar and Fibular Dimelia with Peculiar Facies

4. (1978): Polydactyly as an isolated malformation. In (ed): “The Genetics of Hand Malformations.” New York: Alan R. Liss, Inc., The National Foundation-March of Dimes,

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1. Laurin–Sandrow Syndrome: A Case Report and Review of Literature;The Journal of Hand Surgery (Asian-Pacific Volume);2022-08

2. “Laurin-Sandrow Syndrome – a review of the literature and classification system”;Clinical Dysmorphology;2022-03-07

3. Ulnar Polydactyly and Ulnar Dimelia;Congenital Anomalies of the Upper Extremity;2021

4. Clinical Genetics of Polydactyly: An Updated Review;Frontiers in Genetics;2018-11-06

5. Mirror Foot: A Case Report with Review of Literature;Journal of Foot and Ankle Surgery (Asia Pacific);2018

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