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Publications by Ricarda Flöttmann
Duplication of PTHLH Causes Osteochondroplasia With a Combined Brachydactyly Type E/A1 Phenotype With Disturbed Bone Maturation and Rhizomelia
European Journal of Human Genetics
Genetics
Related publications
A Novel R486Q Mutation in BMPR1B Resulting in Either a Brachydactyly Type C/Symphalangism-Like Phenotype or Brachydactyly Type A2
European Journal of Human Genetics
Genetics
Epilepsy Phenotype in Individuals With Chromosomal Duplication Encompassing FGF12
Epilepsia Open
Neurology
17p13.3 Genomic Rearrangement in a Chinese Family With Split-Hand/Foot Malformation With Long Bone Deficiency: Report of a Complicated Duplication With Marked Variation in Phenotype
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Brachydactyly Type A4
Bone Maturation in Girls With Turner's Syndrome
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Impregnation of Bone Chips With Alendronate and Cefazolin, Combined With Demineralized Bone Matrix: A Bone Chamber Study in Goats
BMC Musculoskeletal Disorders
Rheumatology
Orthopedics
Sports Medicine
A Case of Lipoprotein Glomerulopathy With a Rare Apolipoprotein E Isoform Combined With Neurofibromatosis Type I
CEN Case Reports
Nephrology
Combined Small Cell Lung Carcinoma and Adenocarcinoma With a Neuroendocrine Phenotype
Japanese Journal of Lung Cancer
Oncology
Respiratory Medicine
Pulmonary
Coloboma of Macula-Brachydactyly Type B Syndrome
