131 related articles for article (PubMed ID: 9933333)
1. Hereditary Gottron's acrogeria with recessive transmission: a report of four cases in one family.
Rezai-Delui H; Lotfi N; Mamoori G; Rahimi MB
Pediatr Radiol; 1999 Feb; 29(2):124-30. PubMed ID: 9933333
[TBL] [Abstract][Full Text] [Related]
2. Acrogeria of the Gottron type in a mother and son.
Blaszczyk M; Depaepe A; Nuytinck L; Glinska-Ferenz M; Jablonska S
Eur J Dermatol; 2000; 10(1):36-40. PubMed ID: 10694296
[TBL] [Abstract][Full Text] [Related]
3. Male with type II autosomal recessive cutis laxa.
Imaizumi K; Kurosawa K; Makita Y; Masuno M; Kuroki Y
Clin Genet; 1994 Jan; 45(1):40-3. PubMed ID: 8149651
[TBL] [Abstract][Full Text] [Related]
4. Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation.
Morava E; Lefeber DJ; Urban Z; de Meirleir L; Meinecke P; Gillessen Kaesbach G; Sykut-Cegielska J; Adamowicz M; Salafsky I; Ranells J; Lemyre E; van Reeuwijk J; Brunner HG; Wevers RA
Eur J Hum Genet; 2008 Jan; 16(1):28-35. PubMed ID: 17971833
[TBL] [Abstract][Full Text] [Related]
5. Ambiguous genitalia associated with skeletal abnormalities, cutis laxa, craniostenosis, psychomotor retardation, and facial abnormalities (SCARF syndrome).
Koppe R; Kaplan P; Hunter A; MacMurray B
Am J Med Genet; 1989 Nov; 34(3):305-12. PubMed ID: 2596519
[TBL] [Abstract][Full Text] [Related]
6. [Congenital generalized cutis laxa: 5 cases].
Rybojad M; Baumann C; Godeau G; Moraillon I; Prigent F; Morel P; Bourrat E
Ann Dermatol Venereol; 1999 Apr; 126(4):317-9. PubMed ID: 10421933
[TBL] [Abstract][Full Text] [Related]
7. Cutis laxa of the autosomal recessive type in a consanguineous family.
de Schepper S; Loeys B; de Paepe A; Lambert J; Naeyaert JM
Eur J Dermatol; 2003; 13(6):529-33. PubMed ID: 14721770
[TBL] [Abstract][Full Text] [Related]
8. Skeletal abnormalities of acrogeria, a progeroid syndrome.
Ho A; White SJ; Rasmussen JE
Skeletal Radiol; 1987; 16(6):463-8. PubMed ID: 3659993
[TBL] [Abstract][Full Text] [Related]
9. [Simultaneous occurrence of metageria and Gottron's acrogeria in one family].
Kaufmann I; Thiele B; Mahrle G
Z Hautkr; 1985 Jun; 60(12):975-84. PubMed ID: 4024679
[TBL] [Abstract][Full Text] [Related]
10. Congenital cutis laxa with ligamentous laxity and delayed development, Dandy-Walker malformation and minor heart and osseous defects.
Biver A; De Rijcke S; Toppet V; Ledoux-Corbusier M; Van Maldergem L
Clin Genet; 1994 Jun; 45(6):318-22. PubMed ID: 7523003
[TBL] [Abstract][Full Text] [Related]
11. Craniometadiaphyseal dysplasia, wormian bone type.
Santolaya JM; Hall CM; García-Miñaur S; Delgado A
Am J Med Genet; 1998 May; 77(3):241-5. PubMed ID: 9605592
[TBL] [Abstract][Full Text] [Related]
12. Congenital cutis laxa syndrome: type II autosomal recessive inheritance.
Tüysüz B; Arapoğlu M; Ilikkan B; Demirkesen C; Perk Y
Turk J Pediatr; 2003; 45(3):265-8. PubMed ID: 14696810
[TBL] [Abstract][Full Text] [Related]
13. Yunis-Varon syndrome: the first case of German origin.
Rabe H; Brune T; Rossi R; Steinhorst V; Jorch G; Horst J; Wittwer B
Clin Dysmorphol; 1996 Jul; 5(3):217-22. PubMed ID: 8818450
[TBL] [Abstract][Full Text] [Related]
14. Congenital cutis laxa with retardation of growth and development.
Patton MA; Tolmie J; Ruthnum P; Bamforth S; Baraitser M; Pembrey M
J Med Genet; 1987 Sep; 24(9):556-61. PubMed ID: 3669050
[TBL] [Abstract][Full Text] [Related]
15. Mutations in PYCR1 gene in three families with autosomal recessive cutis laxa, type 2.
Scherrer DZ; Baptista MB; Matos AH; Maurer-Morelli CV; Steiner CE
Eur J Med Genet; 2013 Jun; 56(6):336-9. PubMed ID: 23531708
[No Abstract] [Full Text] [Related]
16. Oto-facio-osseous-gonadal syndrome: a new form of syndromic deafness?
da-Silva EO; Duarte AR; Lins TS
Clin Genet; 1997 Jul; 52(1):51-5. PubMed ID: 9272713
[TBL] [Abstract][Full Text] [Related]
17. [Arterial tortuosity syndrome].
Meyer S; Faiyaz-Ul-Haque M; Zankl M; Sailer NL; Marx N; Limbach HG; Lindinger A
Klin Padiatr; 2005; 217(1):36-40. PubMed ID: 15640971
[TBL] [Abstract][Full Text] [Related]
18. Cutis laxa, intrauterine growth retardation, and bilateral dislocation of the hips: a report of five cases.
Karrar ZA; Elidrissy AT; Adam KA
Prog Clin Biol Res; 1982; 104():215-22. PubMed ID: 6891788
[TBL] [Abstract][Full Text] [Related]
19. Congenital cutis laxa and lysyl oxidase deficiency.
Khakoo A; Thomas R; Trompeter R; Duffy P; Price R; Pope FM
Clin Genet; 1997 Feb; 51(2):109-14. PubMed ID: 9111998
[TBL] [Abstract][Full Text] [Related]
20. De Barsy syndrome--an autosomal recessive, progeroid syndrome.
Kunze J; Majewski F; Montgomery P; Hockey A; Karkut I; Riebel T
Eur J Pediatr; 1985 Nov; 144(4):348-54. PubMed ID: 4076251
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
