Low levels of genetic divergence across geographically and linguistically diverse populations from India von Rosenberg, Noah A, Mahajan, Saurabh, Gonzalez-Quevedo, Catalina, Blum, Michael G B, Nino-Rosales, Laura, Ninis, Vasiliki, Das, Parimal, Hegde, Madhuri, Molinari, Laura, Zapata, Gladys, Weber, James L, Belmont, John W, Patel, Pragna I

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A novel Gln358Glu mutation in ectodysplasin A associated with X-linked dominant incisor hypodontia von Tarpey, Patrick, Pemberton, Trevor J., Stockton, David W., Das, Parimal, Ninis, Vasiliki, Edkins, Sarah, Andrew Futreal, P., Wooster, Richard, Kamath, Sushanth, Nayak, Rabindra, Stratton, Michael R., Patel, Pragna I.

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A new locus for autosomal dominant amelogenesis imperfecta on chromosome 8q24.3 von MENDOZA, Gustavo, PEMBERTON, Trevor J, LEAL, Suzanne M, LINE, Sergio R. P, PATEL, Pragna I, LEE, Kwanghyuk, SCAREL-CAMINAGA, Raquel, MEHRIAN-SHAI, Ruty, GONZALEZ-QUEVEDO, Catalina, NINIS, Vasiliki, HARTIALA, Jaana, ALLAYEE, Hooman, SNEAD, Malcolm L

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Is the novel SCKL3 at 14q23 the predominant Seckel locus? von Kılınç, Mehmet Okyay, Ninis, Vasiliki Ninidu, Uǧur, Sibel Aylin, Tüysüz, Beyhan, Seven, Mehmet, Balcı, Sevim, Goodship, Judith, Tolun, Aslıhan

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Highest heterogeneity for cystic fibrosis: 36 mutations account for 75% of all CF chromosomes in Turkish patients von Kılınç, Mehmet Okyay, Ninis, Vasiliki Ninidu, Dağlı, Elif, Demirkol, Mübeccel, Özkınay, Ferda, Arıkan, Zeliha, Çoğulu, Özgür, Hüner, Gülden, Karakoç, Fazilet, Tolun, Aslıhan

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