Prenatal diagnosis and carrier detection for a point mutation in UBE3A causing Angelman syndrome.

Por Tsai, T F, Raas-Rothschild, A, Ben-Neriah, Z, Beaudet, A L
Publicado em 1998

Refined mapping of a gene for split hand-split foot malformation (SHFM3) on chromosome 10q25.

Por Raas-Rothschild, A, Manouvrier, S, Gonzales, M, Farriaux, J P, Lyonnet, S, Munnich, A
Publicado em 1996

Negative expansion of the myotonic dystrophy unstable sequence.

Por Abeliovich, D, Lerer, I, Pashut-Lavon, I, Shmueli, E, Raas-Rothschild, A, Frydman, M
Publicado em 1993

Pathological features and prenatal diagnosis in the newly recognised limb/pelvis-hypoplasia/aplasia syndrome.

Por Raas-Rothschild, A, Goodman, R M, Meyer, S, Katznelson, M B, Winter, S T, Gross, E, Tamarkin, M, Ben-Ami, T, Nebel, L, Mashiach, S
Publicado em 1988

A Locus for Autosomal Dominant Colobomatous Microphthalmia Maps to Chromosome 15q12-q15

Por Morlé, L., Bozon, M., Zech, J.-C., Alloisio, N., Raas-Rothschild, A., Philippe, C., Lambert, J.-C., Godet, J., Plauchu, H., Edery, P.
Publicado em 2000

Genomic organisation of the UDP-N-acetylglucosamine-1-phosphotransferase gamma subunit (GNPTAG) and its mutations in mucolipidosis III

Por Raas-Rothschild, A, Bargal, R, Goldman, O, Ben-Asher, E, Groener, J, Toutain, A, Stemmer, E, Ben-Neriah, Z, Flusser, H, Beemer, F, Penttinen, M, Olender, T, Rein, A, Bach, G, Zeigler, M
Publicado em 2004