Authors: Al-Saffar, M Lemyre, ME Koenekoop, R Duncan, AMV Kaloustian, VMD

Citation: M. Al-saffar et al., Reply to letter to the editor by Willatt - "Partial trisomy of 2p and neuroblastoma", AM J MED G, 102(3), 2001, pp. 305-305

Authors: Fraser, FC Kaloustian, VMD

Citation: Fc. Fraser et Vmd. Kaloustian, A man, a syndrome, a gene: Clouston's hidrotic ectodermal dysplasia (HED), AM J MED G, 100(2), 2001, pp. 164-168

Authors: Bork, JM Peters, LM Riazuddin, S Bernstein, SL Ahmed, ZM Ness, SL Polomeno, R Ramesh, A Schloss, M Srisailpathy, CRS Wayne, S Bellman, S Desmukh, D Ahmed, Z Khan, SN Kaloustian, VMD Li, XC Lalwani, A Riazuddin, S Bitner-Glindzicz, M Nance, WE Liu, XZ Wistow, G Smith, RJH Griffith, AJ Wilcox, ER Friedman, TB Morell, RJ

Citation: Jm. Bork et al., Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 arecaused by allelic mutations of the novel cadherin-like gene CDH23, AM J HU GEN, 68(1), 2001, pp. 26-37

Authors: Kibar, Z Dube, MP Powell, J McCuaig, C Hayflick, SJ Zonana, J Hovnanian, A Radhakrishna, U Antonarakis, SE Benohanian, A Sheeran, AD Stephan, ML Gosselin, R Kelsell, DP Christianson, AL Fraser, FC Kaloustian, VMD Rouleau, GA

Citation: Z. Kibar et al., Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping, EUR J HUM G, 8(5), 2000, pp. 372-380

Authors: Collins, KA Eydoux, P Duncan, AMV Ortenberg, J Silver, K Kaloustian, VMD

Citation: Ka. Collins et al., Phenotypic manifestation in a child with 46,X,der(X)t(X;1) (q24;q31.1), AM J MED G, 91(5), 2000, pp. 345-347