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Absence Makes the Search Grow Longer

Overview
Journal Am J Hum Genet
Publisher Cell Press
Specialty Genetics
Date 1996 Jan 1
PMID 8554070
Citations 29
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References
1.
Lujan J, Carlin M, Lubs H . A form of X-linked mental retardation with marfanoid habitus. Am J Med Genet. 1984; 17(1):311-22. DOI: 10.1002/ajmg.1320170124. View

2.
Siber M . X-linked recessive microencephaly, microphthalmia with corneal opacities, spastic quadriplesia, hypospadias and cryptorchidism. Clin Genet. 1984; 26(5):453-6. DOI: 10.1111/j.1399-0004.1984.tb01088.x. View

3.
Paetau A, Salonen R, Haltia M . Brain pathology in the Meckel syndrome: a study of 59 cases. Clin Neuropathol. 1985; 4(2):56-62. View

4.
Baverel F, De Recondo J, Rouffet A, Fredy D, Salesses A, Rondot P . [Agenesis of the corpus callosum in a man with complete mosaic trisomy 8]. Presse Med. 1985; 14(14):781-3. View

5.
Kelley R, Datta N, Dobyns W, HAJRA A, Moser A, Noetzel M . Neonatal adrenoleukodystrophy: new cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes. Am J Med Genet. 1986; 23(4):869-901. DOI: 10.1002/ajmg.1320230404. View