Author:
Becker R,Wegner R-D,Kunze J,Runkel S,Vogel M,Entezami M
Subject
Genetics(clinical),Genetics
Reference7 articles.
1. Multiple congenital dislocations associated with characteristic facial abnormality;Larsen;J Pediatr,1950
2. Localization of a gene for autosomal dominant Larsen syndrome to chromosome region 3p21.1-14.1 in the proximity of, but distinct from, the COL7A1 locus;Vujic;Am J Hum Genet,1995
3. Two unrelated children with partial trisomy 1q and monosomy 6p, presenting with the phenotype of the Larsen syndrome;Pierquin;Hum Genet,1991
4. Störungen der Morphogenese: genua recurvata als Deformation bei pathogenetisch unterschiedlichen Fehlbildungs-Syndromen (Larsen-Syndrom, Greig-Polysyndaktylie-Syndrom, partielle Trisomie 10q, Myelomeningocele);Kunze;Klin Pädiat,1984
5. Prenatal diagnosis of recurrent Larsen syndrome: further definition of a lethal variant;Mostello;Prenat Diagn,1991
Cited by
24 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Prenatal and neonatal phenotype of Larsen of La Réunion Island syndrome (B4GALT7-linkeropathy);European Journal of Medical Genetics;2024-06
2. Larsen Syndrome and the Hip;The Pediatric and Adolescent Hip;2019
3. Filamin B: The next hotspot in skeletal research?;Journal of Genetics and Genomics;2017-07
4. Larsen Syndrome;Atlas of Genetic Diagnosis and Counseling;2017
5. Spine;Nursing Care of the Pediatric Neurosurgery Patient;2017