Increased Proportion of Exon 9 Alternatively Spliced CFTR Transcripts in vas Deferens Compared with Nasal Epithelial Cells

By Teng Hui   Jorissen Mark   Van Poppe Hein   Legius Eric   Cassiman Jean-Jacques   Cuppens Harry  

Human Molecular Genetics, Vol. 6, Iss. 1, 1997-01 ,pp. : 85-90

Oxford University Press

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Two Novel Missense Mutations (R766M and R792G) in Exon 13 of the CFTR Gene in a Patient with Congenital Bilateral Absence of the Vas deferens

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Human Heredity, Vol. 50, Iss. 5, 2000-06 ,pp. : 318-319

Karger

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Testicular CFTR splice variants in patients with congenital absence of the vas deferens

By Bassas L.  

Human Molecular Genetics, Vol. 7, Iss. 11, 1998-11 ,pp. : 1739-1743

Oxford University Press

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Functional analysis of cis -acting elements regulating the alternative splicing of human CFTR exon 9

By Niksic Martina   Romano Maurizio   Buratti Emanuele   Pagani Franco   Baralle Francisco E.  

Human Molecular Genetics, Vol. 8, Iss. 13, 1999-12 ,pp. : 2339-2349

Oxford University Press

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Genomic Distribution and Gonadal mRNA Expression of Two Human Luteinizing Hormone Receptor Exon 1 Sequences in Random Populations

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Human Heredity, Vol. 49, Iss. 1, 1999-01 ,pp. : 48-51

Karger

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