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Publications by Xiaolu Meng
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
Related publications
Bilateral Split Hand and Split Foot Malformation in a Boy With a De Novo Interstitial Deletion of 7q21.3
Journal of Medical Genetics
Genetics
Recurrent Streptococcus Pneumoniae Meningitis in a Child With Split Hand and Foot Malformation and Undiagnosed Mondini Dysplasia
Journal of Developmental and Physical Disabilities
Physical Therapy
Sports Therapy
Rehabilitation
Educational Psychology
Developmental
Rare Missense Variant p.Ala505Ser in the ZAK Protein Observed in a Patient With Split-Hand/Foot Malformation From a Non-Consanguineous Pedigree
Journal of International Medical Research
Biochemistry
Medicine
Cell Biology
Marked Intrafamilial Phenotypic Variation in a Family With SOD1 C111Y Mutation
Amyotrophic Lateral Sclerosis
Homozygous Sequence Variants in the WNT10B Gene Underlie Split Hand/Foot Malformation
Genetics and Molecular Biology
Genetics
Molecular Biology
Split Hand/Split Foot Deformity and LADD Syndrome in a Family: Overlap Between the EEC and LADD Syndromes.
Journal of Medical Genetics
Genetics
Iron Deficiency Anemia With Marked Thrombocytosis Complicated by Central Retinal Vein Occlusion
Internal Medicine
Internal Medicine
Medicine
Absent Expression of the Osteoblast-Specific Maternally Imprinted Genes,DLX5andDLX6,causes Split Hand/Split Foot Malformation Type I
Journal of Medical Genetics
Genetics
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
