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Literature DB >> 6011685

[Symmetrical hyperphalangy of the second finger by a supplementary metacarpus bone].

H Manzke.

Abstract

Entities: Disease

Mesh：

Year: 1966 PMID： 6011685

Source DB: PubMed Journal: Fortschr Geb Rontgenstr Nuklearmed ISSN： 0015-8151

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8 in total

1. Brachydactyly type C associated with shortening of the hallux.

Authors: J M Rowe-Jones; A L Moss; M A Patton
Journal: J Med Genet Date: 1992-05 Impact factor: 6.318

2. A male infant with the Catel-Manzke syndrome and dislocatable knees.

Authors: E M Thompson; R M Winter; M J Williams
Journal: J Med Genet Date: 1986-06 Impact factor: 6.318

3. Pierre Robin syndrome with hyperphalangism-clinodactylysm of the index finger: a possible new palato-digital syndrome.

Authors: M C Silengo; P Franceschini; A Cerutti; C Fabris
Journal: Pediatr Radiol Date: 1977-10-28

4. Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome.

Authors: Nadja Ehmke; Almuth Caliebe; Rainer Koenig; Sarina G Kant; Zornitza Stark; Valérie Cormier-Daire; Dagmar Wieczorek; Gabriele Gillessen-Kaesbach; Kirstin Hoff; Amit Kawalia; Holger Thiele; Janine Altmüller; Björn Fischer-Zirnsak; Alexej Knaus; Na Zhu; Verena Heinrich; Celine Huber; Izabela Harabula; Malte Spielmann; Denise Horn; Uwe Kornak; Jochen Hecht; Peter M Krawitz; Peter Nürnberg; Reiner Siebert; Hermann Manzke; Stefan Mundlos
Journal: Am J Hum Genet Date: 2014-12-04 Impact factor: 11.025

[Symmetrical hyperphalangy of the second finger by a supplementary metacarpus bone].

1. Brachydactyly type C associated with shortening of the hallux.

2. A male infant with the Catel-Manzke syndrome and dislocatable knees.

3. Pierre Robin syndrome with hyperphalangism-clinodactylysm of the index finger: a possible new palato-digital syndrome.

4. Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome.

5. Cleft palate and accessory metacarpal of index finger syndrome: possible familial occurrence.

6. Pierre Robin sequence and hyperphalangy--a genetic entity (Catel-Manzke syndrome).

7. Trisomy 10qter confirmed by in situ hybridisation.

8. Catel-Manzke Syndrome: Further Delineation of the Phenotype Associated with Pathogenic Variants in TGDS.