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Genetic heterogeneity and exclusion of a modifying locus at 2q in a family with autosomal dominant primary erythermalgia

✍ Scribed by T.M. Burns; R.H.M. Te Morsche; J.B.M.J. Jansen; J.P. H. Drenth

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Autosomal dominant infant GERD: Exclusio

✍ Orenstein, Susan R.; Shalaby, Theresa M.; Pfuetzer, Roland H.; Michael Barmada, 📂 Article 📅 2001 🏛 Elsevier Science 🌐 English ⚖ 176 KB

Confirmation of linkage to 1q21-31 in a

✍ Caroline Graff; Steen F. Urbak; Tord Jerndal; Claes Wadelius 📂 Article 📅 1995 🏛 Springer 🌐 English ⚖ 870 KB

Exclusion of chromosome 6 and 8 location

✍ Bashir, R.; Inglehearn, C.F.; Keen, T.J.; Lindsey, J.; Atif, U.; Carter, S.A.; S 📂 Article 📅 1992 🏛 Elsevier Science 🌐 English ⚖ 232 KB

Refinement of a locus for autosomal domi

✍ Kouji Maeda; Ryuji Kaji; Katsuhito Yasuno; Jamiyansuren Jambaldorj; Hiroyuki Nod 📂 Article 📅 2007 🏛 Nature Publishing Group 🌐 English ⚖ 333 KB

Exclusion of Chromosome Regions 6p12 and

✍ C. Klein; P. Vieregge; W. Heide; B. Kemper; M. Hagedorn-Greiwe; J. Hagenah; C. V 📂 Article 📅 1998 🏛 Elsevier Science 🌐 English ⚖ 40 KB

Microphthalmos in the presumed homozygou

✍ Bodker, Fred S. ;Lavery, Mary Ann ;Mitchell, Thomas N. ;Lovrien, Everett W. ;Mau 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 604 KB