L I al-Gazali

Two 46,XX,t(X;Y) females with linear skin defects and congenital microphthalmia: a new syndrome at Xp22.3.

L I al-Gazali, R F Mueller, A. Caine et al. · Journal of Medical Genetics · 1990 · 101 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22.

David A. Campbell, Duncan P. McHale, Kathryn Brown et al. · Journal of Medical Genetics · 1997 · 57 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

The oculocerebrocutaneous (Delleman) syndrome.

L I al-Gazali, Dian Donnai, Susan A. Berry et al. · Journal of Medical Genetics · 1988 · 53 citations · Full text

Medicine, Ophthalmology, Pediatrics +14

Diagnostic and counselling difficulties using a fully comprehensive screening protocol for families at risk for tuberous sclerosis.

L I al-Gazali, R. J. Arthur, J T Lamb et al. · Journal of Medical Genetics · 1989 · 19 citations · Full text

Life Sciences, Genetics, Family Assessment +15

Hirschsprung's disease, hypoplastic nails, and minor dysmorphic features: a distinct autosomal recessive syndrome?

L I al-Gazali, Dian Donnai, Rebecca Mueller · Journal of Medical Genetics · 1988 · 13 citations · Full text

Life Sciences, Genetics, Pediatrics +10