Two sibs with unbalanced translocations in the Waardenburg gene region.

Por al Gazali, L I, Quaife, R
Publicado em 1993

A syndrome of insulin resistance resembling leprechaunism in five sibs of consanguineous parents.

Por al-Gazali, L I, Khalil, M, Devadas, K
Publicado em 1993

A syndrome of immune complex glomerulonephritis and ophthalmic abnormalities

Por Amirlak, I., Sabnis, S., Al-Gazali, L., Abdulrazzaq, Y.
Publicado em 1999

Bilateral retinopathy, aplastic anaemia, and central nervous system abnormalities: a new syndrome?

Por Revesz, T, Fletcher, S, al-Gazali, L I, DeBuse, P
Publicado em 1992

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

Por al-Gazali, L I, Donnai, D, Mueller, R F
Publicado em 1988

The profile of major congenital abnormalities in the United Arab Emirates (UAE) population.

Por al-Gazali, L I, Dawodu, A H, Sabarinathan, K, Varghese, M
Publicado em 1995

Absent pituitary gland and hypoplasia of the cerebellar vermis associated with partial ophthalmoplegia and postaxial polydactyly: a variant of orofaciodigital syndrome VI or a new...

Por Al-Gazali, L, Sztriha, L, Punnose, J, Shather, W, Nork, M
Publicado em 1999

A Novel Aberrant Splice Site Mutation in RAB23 Leads to an Eight Nucleotide Deletion in the mRNA and Is Responsible for Carpenter Syndrome in a Consanguineous Emirati Family

Por Ben-Salem, S., Begum, M.A., Ali, B.R., Al-Gazali, L.
Publicado em 2013

Further delineation of Nevo syndrome.

Por al-Gazali, L I, Bakalinova, D, Varady, E, Scorer, J, Nork, M
Publicado em 1997

Homozygosity for a new mutation (Ile119-->Met) in the insulin receptor gene in five sibs with familial insulin resistance.

Por Hone, J, Accili, D, al-Gazali, L I, Lestringant, G, Orban, T, Taylor, S I
Publicado em 1994

The oculocerebrocutaneous (Delleman) syndrome.

Por al-Gazali, L I, Donnai, D, Berry, S A, Say, B, Mueller, R F
Publicado em 1988

Wolcott-Rallison syndrome: pathogenic insights into neonatal diabetes from new mutation and expression studies of EIF2AK3

Por Brickwood, S, Bonthron, D, Al-Gazali, L, Piper, K, Hearn, T, Wilson, D, Hanley, N
Publicado em 2003

A novel mutation in a family with non-syndromic sensorineural hearing loss that disrupts the newly characterised OTOF long isoforms

Por Houseman, M., Jackson, A., Al-Gazali, L., Badin, R., Roberts, E., Mueller, R.
Publicado em 2001

The spectrum of beta thalassaemia mutations in the UAE national population.

Por Quaife, R, al-Gazali, L, Abbes, S, Fitzgerald, P, Fitches, A, Valler, D, Old, J M
Publicado em 1994

Organisation of the human PAX4 gene and its exclusion as a candidate for the Wolcott-Rallison syndrome.

Por Bonthron, D T, Dunlop, N, Barr, D G, El Sanousi, A A, Al-Gazali, L I
Publicado em 1998

Neonatal Schwartz-Jampel syndrome: a common autosomal recessive syndrome in the United Arab Emirates.

Por Al-Gazali, L I, Varghese, M, Varady, E, Al Talabani, J, Scorer, J, Bakalinova, D
Publicado em 1996

Complex consanguinity associated with short rib-polydactyly syndrome III and congenital infection-like syndrome: a diagnostic problem in dysmorphic syndromes

Por Al-Gazali, L, Sztriha, L, Dawodu, A, Varady, E, Bakir, M, Khdir, A, Johansen, J
Publicado em 1999

The Schinzel-Giedion syndrome.

Por al-Gazali, L I, Farndon, P, Burn, J, Flannery, D B, Davison, C, Mueller, R F
Publicado em 1990

Diagnostic criteria, clinical characteristics, and natural history of Cohen syndrome

Por Chandler, K, Kidd, A, Al-Gazali, L, Kolehmainen, J, Lehesjoki, A, Black, G, Clayton-Smith, J
Publicado em 2003

Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26

Por Bayoumi, R., Saar, K., Lee, Y., Nurnberg, G., Reis, A., Nur-E-Kamal, M., Al-Gazali, L.
Publicado em 2001