I K Jalili

Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta

David Parry, Alan J. Mighell, Walid El‐Sayed et al. · The American Journal of Human Genetics · 2009 · 166 citations · Full text

A progressive cone-rod dystrophy and amelogenesis imperfecta: a new syndrome.

I K Jalili, Natasha Smith · Journal of Medical Genetics · 1988 · 77 citations · Full text

Cone-rod congenital amaurosis associated with congenital hypertrichosis: an autosomal recessive condition.

I K Jalili · Journal of Medical Genetics · 1989 · 42 citations · Full text

Developmental Anomaly, Ocular Disease, Ophthalmology +13

Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregate

Louise Downey, T J Keen, I K Jalili et al. · European Journal of Human Genetics · 2002 · 36 citations · Full text

Biology, Developmental Biology, Mendelian Disorder +11

Cone-rod dystrophy and amelogenesis imperfecta (Jalili syndrome): phenotypes and environs

I K Jalili · Eye · 2010 · 35 citations · Full text

Developmental Anomaly, Developmental Biology, Jalili Syndrome +5