These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
44. X-mapping in man: evidence against measurable linkage between anhidrotic ectodermal dysplasia and G6PD deficiency. Filippi G; Rinaldi A; Crisponi G; Daniels GL; Siniscalco M J Med Genet; 1979 Jun; 16(3):223-4. PubMed ID: 469901 [TBL] [Abstract][Full Text] [Related]
45. A Novel Locus for Ectodermal Dysplasia of Hair, Nail and Skin Pigmentation Anomalies Maps to Chromosome 18p11.32-p11.31. Habib R; Ansar M; Mattheisen M; Shahid M; Ali G; Ahmad W; Betz RC PLoS One; 2015; 10(6):e0129811. PubMed ID: 26115030 [TBL] [Abstract][Full Text] [Related]
46. A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO). Zonana J; Elder ME; Schneider LC; Orlow SJ; Moss C; Golabi M; Shapira SK; Farndon PA; Wara DW; Emmal SA; Ferguson BM Am J Hum Genet; 2000 Dec; 67(6):1555-62. PubMed ID: 11047757 [TBL] [Abstract][Full Text] [Related]
49. Characterisation of molecular DNA rearrangements within the Xq12-q13.1 region, in three patients with X-linked hypohidrotic ectodermal dysplasia (EDA). Thomas NS; Chelly J; Zonana J; Davies KJ; Morgan S; Gault J; Rack KA; Buckle VJ; Brockdorff N; Clarke A Hum Mol Genet; 1993 Oct; 2(10):1679-85. PubMed ID: 8268921 [TBL] [Abstract][Full Text] [Related]
50. Recognition and reanalysis of a cell line from a manifesting female with X linked hypohidrotic ectodermal dysplasia and an X; autosome balanced translocation. Zonana J; Roberts SH; Thomas NS; Harper PS J Med Genet; 1988 Jun; 25(6):383-6. PubMed ID: 3398005 [TBL] [Abstract][Full Text] [Related]
51. Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation. Rasool M; Nawaz S; Azhar A; Wajid M; Westermark P; Baig SM; Klar J; Dahl N Eur J Dermatol; 2010; 20(4):443-6. PubMed ID: 20409997 [TBL] [Abstract][Full Text] [Related]
52. Dermatoglyphics findings in families with X-linked hypohidrotic(or anhidrotic) ectodermal dysplasia(HED). Rodewald A; Zahn-Messow K Prog Clin Biol Res; 1982; 84():451-8. PubMed ID: 6896579 [TBL] [Abstract][Full Text] [Related]
53. Autosomal dominant hypohidrotic ectodermal dysplasia in a large family. Aswegan AL; Josephson KD; Mowbray R; Pauli RM; Spritz RA; Williams MS Am J Med Genet; 1997 Nov; 72(4):462-7. PubMed ID: 9375732 [TBL] [Abstract][Full Text] [Related]
54. Genetic mapping of canine multiple system degeneration and ectodermal dysplasia loci. O'Brien DP; Johnson GS; Schnabel RD; Khan S; Coates JR; Johnson GC; Taylor JF J Hered; 2005; 96(7):727-34. PubMed ID: 15958791 [TBL] [Abstract][Full Text] [Related]
55. Clinical and radiographic dental findings in X linked hypohidrotic ectodermal dysplasia. Crawford PJ; Aldred MJ; Clarke A J Med Genet; 1991 Mar; 28(3):181-5. PubMed ID: 2051453 [TBL] [Abstract][Full Text] [Related]
56. TP63 mutation and clefting modifier genes in an EEC syndrome family. Ray AK; Marazita ML; Pathak R; Beever CL; Cooper ME; Goldstein T; Shaw DF; Field LL Clin Genet; 2004 Sep; 66(3):217-22. PubMed ID: 15324320 [TBL] [Abstract][Full Text] [Related]
57. Growth hormone neurosecretory dysfunction in a boy with hypohidrotic/anhidrotic ectodermal dysplasia: definition of short stature, molecular characterization and long-term hGH replacement treatment to final height. Stagi S; Lapi E; Sani I; Bindi G; Quaranta MR; Salti R; Chiarelli F J Pediatr Endocrinol Metab; 2009 Sep; 22(9):853-8. PubMed ID: 19960895 [TBL] [Abstract][Full Text] [Related]
58. [Ectodermal anhidrotic dysplasia in 3 brothers and their 1st cousin]. Lapière S; Dodinval P Ann Dermatol Syphiligr (Paris); 1967; 94(5):477-89. PubMed ID: 5586823 [No Abstract] [Full Text] [Related]
59. [Syndromes 17. Hypohidrotic ectodermal dysplasia]. Baart JA; van Hagen JM Ned Tijdschr Tandheelkd; 2000 Jan; 107(1):12-4. PubMed ID: 12621820 [TBL] [Abstract][Full Text] [Related]
60. [Anhidrotic ectodermal dysplasia: two cases in a family]. Song YX; Yang S; Lin D; Li M; Ge HS; Zhang XJ Zhonghua Er Ke Za Zhi; 2003 Apr; 41(4):289. PubMed ID: 14754537 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]