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Possible relationship between the van der Woude syndrome (vWS) locus and nonsyndromic cleft lip with or without cleft palate (NSCL/P).

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Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes.

A. Ziegler, K. Grzeschik, G. Rizzoni, 1997, Human molecular genetics.

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Identification of three novel mutations in the CFTR gene, R117P, ΔD192, and 3121‐1G→A in four French patients

P. Aymard, A. Sardet, G. Tournier, 1998 .