Publisher
Springer Berlin Heidelberg
Reference238 articles.
1. Abdel-Al YK, Shabani IS, Lubani MM, Al-Ghanem MA, Ibrahim MD, Al-Mohtaseb S, Duodin K (1994) Autosomal recessive osteopetrosis in Arab children. Ann Trop Paediatr 14:59–64
2. Abdul Wahab A, Al-Thani G, Dawod ST, Kambouris M, Al-Hamed M (2001) Heterogeneity of the cystic fibrosis phenotype in a large kindred family in Qatar with cystic fibrosis mutation (I1234V). J Trop Pediatr 47:110–112
3. Abeliovich D, Atia Y, Sarov B (1986) Down syndome in Negev region. Am J Med Genet 25:183
4. Abeliovich D, Lavon IP, Lerer I, Cohen T, Springer C, Avital A, Cuttnig GR (1992) Screening for five mutations detects 97% of Cystic Fibrosis (CF) chromosomes and predicts a carrier frequency of 1:29 in The Jewish Ashkenazi population. Am J Hum Genet 51:951–956
5. Abu-Osba YK, Mallouh A, Salaman M, Hann R, Thalji A, Hamdan J, Sa’di AR (1992) Comprehensive newborn screening program: Aramco experience, the national need and recommendations. Ann Saudi Med 132:235–240
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