A. Grillo

The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regions.

A. C. Chinault, A. Ballabio, H. Zoghbi, 1993, Human molecular genetics.

Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization.

H. Zoghbi, A. Baldini, M. Grompe, 1994, American journal of medical genetics.

Major COL4A5 gene rearrangements in patients with juvenile type Alport syndrome.

A. Ballabio, G. Rizzoni, F. Scolari, 1995, American journal of medical genetics.

A high resolution deletion map of human chromosome Xp22

T. Mohandas, A. Ballabio, H. Zoghbi, 1993, Nature Genetics.

A gene from the Xp22.3 region shares homology with voltage-gated chloride channels.

G. Borsani, E. Rugarli, A. Ballabio, 1994, Human molecular genetics.

Noninvasive prenatal diagnosis of chromosomal aneuploidies by isolation and analysis of fetal cells from maternal blood.

H. Takabayashi, P. Pavone, E. Parano, 2001, American journal of medical genetics.

Fetal nucleated red blood cell counts in peripheral blood of mothers bearing Down syndrome fetus.

H. Takabayashi, P. Pavone, E. Parano, 2001, Neuropediatrics.