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Publications by Arti Nanda

Mutations in GRHL2 Result in an Autosomal-Recessive Ectodermal Dysplasia Syndrome

American Journal of Human Genetics

English

Clinical, Immunologic and Genetic Profiles of DOCK8-deficient Patients in Kuwait

Clinical Immunology

English

Related publications

Loss-Of-Function Mutations in HPSE2 Cause the Autosomal Recessive Urofacial Syndrome

American Journal of Human Genetics

English

Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability

American Journal of Human Genetics

English

Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts

American Journal of Human Genetics

English

Cerebellar Ataxia-Ectodermal Dysplasia Syndrome

English

Ectodermal Dysplasia-Sensorineural Deafness Syndrome

English

Newly Discovered Mutations in the GALNT3 Gene Causing Autosomal Recessive Hyperostosis-Hyperphosphatemia Syndrome

Acta Orthopaedica

Sports Medicine

English

Mutations in EOGT Confirm the Genetic Heterogeneity of Autosomal-Recessive Adams-Oliver Syndrome

American Journal of Human Genetics

English

Acrocapitofemoral Dysplasia: An Autosomal Recessive Skeletal Dysplasia With Cone Shaped Epiphyses in the Hands and Hips

Journal of Medical Genetics

English

Autosomal Recessive Chorioretinopathy-Microcephaly Syndrome

English