| Unbound MEDLINE results for: | Bookmark this site | | Articles related to 474638 [Unique ID], provided by the PubMed system | |
| |
|
| | 1 - 10 of 101 journal articles in the PubMed database | Email to a friend | | |
| Lisker R, Hernández A, Martínez-Lavin M, et al.
Gerodermia osteodysplastica hereditaria: report of three affected brothers and literature review. [Case Reports, Journal Article]
Am J Med Genet 1979; 3(4):389-95.
Abstract | Full Citation | Find Related Articles | | Nanda A, Alsaleh QA, Al-Sabah H, et al.
Gerodermia Osteodysplastica/Wrinkly Skin Syndrome: Report of Three Patients and Brief Review of the Literature. [JOURNAL ARTICLE]
Pediatr Dermatol 2008 Jan; 25(1):66-71.
Abstract | Full Citation | Find Related Articles | | Al-Gazali LI, Sztriha L, Skaff F, et al.
Gerodermia osteodysplastica and wrinkly skin syndrome: are they the same? [Case Reports, Journal Article]
Am J Med Genet 2001 Jul 1; 101(3):213-20.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Hunter AG, Martsolf JT, Baker CG, et al.
Geroderma osteodysplastica. A report of two affected families. [Journal Article]
Hum Genet 1978 Feb 16; 40(3):311-24.
Abstract | Full Citation | Find Related Articles | | Sayli BS, Gül D
GAPO syndrome in three relatives in a Turkish kindred. [Case Reports, Journal Article]
Am J Med Genet 1993 Sep 1; 47(3):342-5.
Abstract | Full Citation | Find Related Articles | | Dallaire L, Cantin M, Melançon SB, et al.
A syndrome of generalized elastic fiber deficiency with leprechaunoid features: a distinct genetic disease with an autosomal recessive mode of inheritance. [Case Reports, Journal Article]
Clin Genet 1976 Jul; 10(1):1-11.
Abstract | Full Citation | Find Related Articles | | Rajab A, Kornak U, Budde BS, et al.
Geroderma osteodysplasticum hereditaria and wrinkly skin syndrome in 22 patients from Oman. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Mar 17.
Abstract | Full Citation | Find Related Articles | | Teebi AS
Autosomal recessive Robinow syndrome. [Case Reports, Journal Article]
Am J Med Genet 1990 Jan; 35(1):64-8.
Abstract | Full Citation | Find Related Articles | | Pallotta R, Morgese G
Mandibuloacral dysplasia: a rare progeroid syndrome. Two brothers confirm autosomal recessive inheritance. [Case Reports, Journal Article]
Clin Genet 1984 Aug; 26(2):133-8.
Abstract | Full Citation | Find Related Articles |   |
|
| |
Advertise on this site.
|
