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.
180 related articles for article (PubMed ID: 6482910)
1. Inherited chondrodysplasia punctata due to a deletion of the terminal short arm of an X chromosome. Curry CJ; Magenis RE; Brown M; Lanman JT; Tsai J; O'Lague P; Goodfellow P; Mohandas T; Bergner EA; Shapiro LJ N Engl J Med; 1984 Oct; 311(16):1010-5. PubMed ID: 6482910 [TBL] [Abstract][Full Text] [Related]
2. Deletion of the distal short arm of the X chromosome (Xp) in a patient with short stature, chondrodysplasia punctata, and X-linked ichthyosis due to steroid sulfatase deficiency. Ballabio A; Zollo M; Carrozzo R; Caiulo A; Zuffardi O; Cascioli CF; Viggiano D; Strisciuglio P Am J Med Genet; 1991 Nov; 41(2):184-7. PubMed ID: 1785631 [TBL] [Abstract][Full Text] [Related]
3. Familial X-linked ichthyosis, steroid sulfatase deficiency, mental retardation, and nullisomy for Xp223-pter. Ross JB; Allderdice PW; Shapiro LJ; Aveling J; Eales BA; Simms D Arch Dermatol; 1985 Dec; 121(12):1524-8. PubMed ID: 3864397 [TBL] [Abstract][Full Text] [Related]
4. Absent chondrodysplasia punctata in a male with an Xp terminal deletion involving the putative region for CDPX1 locus. Ogata T; Goodfellow P; Petit C; Maroteaux P; Matsuo N Am J Med Genet; 1993 Jan; 45(1):101-4. PubMed ID: 8418639 [TBL] [Abstract][Full Text] [Related]
5. Detection of gene deletions in children with chondrodysplasia punctata, ichthyosis, Kallmann syndrome, and ocular albinism by FISH studies. Hou JW Chang Gung Med J; 2005 Sep; 28(9):643-50. PubMed ID: 16323556 [TBL] [Abstract][Full Text] [Related]
6. X/Y translocation in a family with X-linked ichthyosis, chondrodysplasia punctata, and mental retardation: DNA analysis reveals deletion of the steroid sulphatase gene and translocation of its Y pseudogene. Ballabio A; Parenti G; Carrozzo R; Coppa G; Felici L; Migliori V; Silengo M; Franceschini P; Andria G Clin Genet; 1988 Jul; 34(1):31-7. PubMed ID: 3165728 [TBL] [Abstract][Full Text] [Related]
7. Male infant with ichthyosis, Kallmann syndrome, chondrodysplasia punctata, and an Xp chromosome deletion. Bick D; Curry CJ; McGill JR; Schorderet DF; Bux RC; Moore CM Am J Med Genet; 1989 May; 33(1):100-7. PubMed ID: 2750777 [TBL] [Abstract][Full Text] [Related]
8. X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosome. Ballabio A; Parenti G; Tippett P; Mondello C; Di Maio S; Tenore A; Andria G Hum Genet; 1986 Mar; 72(3):237-40. PubMed ID: 3007328 [TBL] [Abstract][Full Text] [Related]
9. Two cases of steroid sulfatase deficiency with complex phenotype due to contiguous gene deletions. Nishimura S; Masuda H; Matsumoto T; Sakura N; Matsumoto T; Ueda K Am J Med Genet; 1991 Sep; 40(3):260-3. PubMed ID: 1951426 [TBL] [Abstract][Full Text] [Related]
10. Chondrodysplasia punctata: a boy with X-linked recessive chondrodysplasia punctata due to an inherited X-Y translocation with a current classification of these disorders. Wulfsberg EA; Curtis J; Jayne CH Am J Med Genet; 1992 Jul; 43(5):823-8. PubMed ID: 1642270 [TBL] [Abstract][Full Text] [Related]
11. X-linked dominant chondrodysplasia punctata/ichthyosis/cataract syndrome in males. Happle R Am J Med Genet; 1995 Jul; 57(3):493. PubMed ID: 7677158 [No Abstract] [Full Text] [Related]
12. Prenatal findings in a fetus with contiguous gene syndrome caused by deletion of Xp22.3 that includes locus for X-linked recessive type of chondrodysplasia punctata (CDPX1). Horikoshi T; Kikuchi A; Tamaru S; Ono K; Kita M; Takagi K; Miyashita S; Kawame H; Shimokawa O; Harada N J Obstet Gynaecol Res; 2010 Jun; 36(3):671-5. PubMed ID: 20598055 [TBL] [Abstract][Full Text] [Related]
13. Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223. Tiepolo L; Zuffardi O; Fraccaro M; di Natale D; Gargantini L; Müller CR; Ropers HH Hum Genet; 1980; 54(2):205-6. PubMed ID: 6930361 [TBL] [Abstract][Full Text] [Related]
14. Brachytelephalangic chondrodysplasia punctata: a possible X-linked recessive form. Maroteaux P Hum Genet; 1989 May; 82(2):167-70. PubMed ID: 2722194 [TBL] [Abstract][Full Text] [Related]
15. X-linked dominant chondrodysplasia punctata: a case report and family studies. Mueller RF; Crowle PM; Jones RA; Davison BC Am J Med Genet; 1985 Jan; 20(1):137-44. PubMed ID: 4038582 [TBL] [Abstract][Full Text] [Related]
16. Skewed X-chromosome inactivation causes intra-familial phenotypic variation of an EBP mutation in a family with X-linked dominant chondrodysplasia punctata. Shirahama S; Miyahara A; Kitoh H; Honda A; Kawase A; Yamada K; Mabuchi A; Kura H; Yokoyama Y; Tsutsumi M; Ikeda T; Tanaka N; Nishimura G; Ohashi H; Ikegawa S Hum Genet; 2003 Jan; 112(1):78-83. PubMed ID: 12483303 [TBL] [Abstract][Full Text] [Related]
17. Short stature in a mother and daughter with terminal deletion of Xp22.3. Schwinger E; Kirschstein M; Greiwe M; Konermann T; Orth U; Gal A Am J Med Genet; 1996 May; 63(1):239-42. PubMed ID: 8723116 [TBL] [Abstract][Full Text] [Related]
18. A patient with an interstitial deletion in Xp22.3 locates the gene for X-linked recessive chondrodysplasia punctata to within a one megabase interval. Klink A; Meindl A; Hellebrand H; Rappold GA Hum Genet; 1994 Apr; 93(4):463-6. PubMed ID: 8168818 [TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis and investigation of a fetus with chondrodysplasia punctata, ichthyosis, and Kallmann syndrome due to an Xp deletion. Bick DP; Schorderet DF; Price PA; Campbell L; Huff RW; Shapiro LJ; Moore CM Prenat Diagn; 1992 Jan; 12(1):19-29. PubMed ID: 1557308 [TBL] [Abstract][Full Text] [Related]
20. X-linked dominant chondrodysplasia punctata (CDPX2): multisystemic impact of the defect in cholesterol biosynthesis. Martanová H; Krepelová A; Baxová A; Hansíková H; Cánský Z; Kvapil M; Gregor V; Magner M; Zeman J Prague Med Rep; 2007; 108(3):263-9. PubMed ID: 18399064 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]