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Clinical Genetics|February 1, 2014
The communication of secondary variants: interviews with parents whose children have undergone array-CGH testingG M Christenhusz, K Devriendt, H Peeters, et al.
Clinical Genetics|November 1, 1996
Variable clinical expression in a family with OI type IV due to deletion of three base pairs in COL1A1A M Lund, M Schwartz, F Skovby
Clinical Genetics|November 1, 1996
Prenatal diagnosis of terminal deletion 7q and partial trisomy 3p in fetuses with holoprosencephalyC P Chen, F F Liu, S W Jan, et al.
Clinical Genetics|November 1, 1996
Cord blood immunoglobulin E in like-sexed monozygotic and dizygotic twinsS Husby, N V Holm, K Christensen, et al.
Clinical Genetics|November 1, 1996
Routine clinical application of the FRAXA Pfu PCR assay: limits and utilityD F Condorelli, G Milana, P Dell'Albani, et al.
Clinical Genetics|November 1, 1996
Autosomal recessive retinitis pigmentosa in Spain: evaluation of four genes and two loci involved in the diseaseM Bayés, A Martínez-Mir, D Valverde, et al.
Clinical Genetics|November 1, 1996
Discordant monozygotic twins with the Schimmelpenning-Feuerstein-Mims syndromeH D Schworm, K B Jedele, E Holinski, et al.
Clinical Genetics|November 1, 1996
Report of a new case of axial mesodermal dysplasia complexR Bini, D A Danti, M Materassi, et al.
Clinical Genetics|October 1, 1996
DNA testing in familial hypertrophic cardiomyopathy: clinical and laboratory implicationsR V Smart, B Yu, H Le, et al.
Clinical Genetics|October 1, 1996
Nonsyndromic X-linked mental retardation: review and mapping of MRX29 to Xp21B Häne, R J Schroer, J F Arena, et al.
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