The autosomal recessive variety of congenital stationary night-blindness with myopia.

Por Der Kaloustian, V M, Baghdassarian, S A
Publicado em 1972

Severe intrauterine growth retardation with increased mitomycin C sensitivity, or Nijmegen breakage syndrome?

Por Der Kaloustian, V M, Elliott, A M, Eydoux, P
Publicado em 1995

Psychosocial and economic profile of a sample of families with thalassaemic children in Lebanon.

Por Der Kaloustian, V M, Khudr, A, Firzli, S, Dabbous, I
Publicado em 1987

Atypical serum cholinesterase in a family with congenital distichiasis.

Por Shammas, H F, Tabbara, K F, der Kaloustian, V M
Publicado em 1976

Evidence for a fourth locus in Usher syndrome type I.

Por Gerber, S, Larget-Piet, D, Rozet, J M, Bonneau, D, Mathieu, M, Der Kaloustian, V, Munnich, A, Kaplan, J
Publicado em 1996

Five related Lebanese individuals with high plasma lysosomal hydrolases: a new defect in mannose-6-phosphate receptor recognition?

Por Alexander, D, Dudin, G, Talj, F, Bitar, F, Deeb, M, Khudr, A, Abboud, M, Der Kaloustian, V M
Publicado em 1984

Linkage analysis of the nail-patella syndrome.

Por Campeau, E, Watkins, D, Rouleau, G A, Babul, R, Buchanan, J A, Meschino, W, Der Kaloustian, V M
Publicado em 1995

Translocation between chromosomes 6 and 15 (45,XX,t(6;15)(q25;q11.2)) with further evidence for lack of imprinting of the insulin-like growth factor II/mannose-6-phosphate receptor...

Por Treacy, E, Polychronakos, C, Vekemans, M, Eydoux, P, Blaichman, S, Scarpelli, H, Ross, M, Xu, Y, Der Kaloustian, V M
Publicado em 1996

Sandhoff disease: a prevalent form of infantile GM2 gangliosidosis in Lebanon.

Por Der Kaloustian, V M, Khoury, M J, Hallal, R, Idriss, Z H, Deeb, M E, Wakid, N W, Haddad, F S
Publicado em 1981

An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.

Por Mitchell, G A, Brody, L C, Looney, J, Steel, G, Suchanek, M, Dowling, C, Der Kaloustian, V, Kaiser-Kupfer, M, Valle, D
Publicado em 1988

Silencing of CDKN1C (p57(KIP2)) is associated with hypomethylation at KvDMR1 in Beckwith–Wiedemann syndrome

Por Diaz-Meyer, N, Day, C, Khatod, K, Maher, E, Cooper, W, Reik, W, Junien, C, Graham, G, Algar, E, Der Kaloustian, V M, Higgins, M
Publicado em 2003

Severe forms of Baraitser–Winter syndrome are caused by ACTB mutations rather than ACTG1 mutations

Por Di Donato, N, Rump, A, Koenig, R, Der Kaloustian, V M, Halal, F, Sonntag, K, Krause, C, Hackmann, K, Hahn, G, Schrock, E, Verloes, A
Publicado em 2014

Molecular Analysis of Collagen XVIII Reveals Novel Mutations, Presence of a Third Isoform, and Possible Genetic Heterogeneity in Knobloch Syndrome

Por Suzuki, O. T., Sertié, A. L., Der Kaloustian, V. M., Kok, F., Carpenter, M., Murray, J., Czeizel, A. E., Kliemann, S. E., Rosemberg, S., Monteiro, M., Olsen, B. R., Passos-Bueno, M. R.
Publicado em 2002