Further evidence for FGF16 truncating mutations as the cause of X‐linked recessive fusion of metacarpals 4 / 5-Reference-Cited by-同舟云学术

Further evidence for FGF16 truncating mutations as the cause of X‐linked recessive fusion of metacarpals 4 / 5

Published:2014-04 Issue:4 Volume:100 Page:314-318
ISSN:1542-0752
Container-title:Birth Defects Research Part A: Clinical and Molecular Teratology
language:en
Short-container-title:Birth Defects Research

Author:

Jamsheer Aleksander¹²,Śmigiel Robert³,Jakubiak Aleksandra⁴,Zemojtel Tomasz⁵⁶,Socha Magdalena¹,Robinson Peter N.⁶,Mundlos Stefan⁶⁷⁸

Affiliation:

1. Department of Medical GeneticsPoznan University of Medical SciencesPoznan Poland

2. NZOZ Center for Medical Genetics GENESISPoznan Poland

3. Department of Pediatrics and Rare DisordersWroclaw Medical UniversityWroclaw Poland

4. Department of GeneticsWroclaw Medical UniversityWroclaw Poland

5. Institute of Bioorganic Chemistry, Polish Academy of SciencesPoznan Poland

6. Institute for Medical Genetics and Human Genetics, Charité‐Universitätsmedizin BerlinBerlin Germany

7. Max Planck Institute for Molecular GeneticsBerlin Germany

8. Berlin‐Brandenburg Center for Regenerative Therapies (BCRT)Charité‐Universitätsmedizin BerlinBerlin Germany

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology and Child Health

Link

Reference18 articles.

2. Familial synostosis of metacarpi IV and V;Habighorst LV;Z Orthop Ihre Grenzgeb,1965

3. Metacarpal 4‐5 fusion with X‐linked recessive inheritance;Holmes LB;Am J Hum Genet,1972

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