179 related articles for article (PubMed ID: 8166424)
1. X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome. Report of three male patients in a large French family.
Lefort G; Taib J; Toutain A; Houdayer C; Moraine CI; Humeau C; Sarda P
Ann Genet; 1993; 36(4):200-5. PubMed ID: 8166424
[TBL] [Abstract][Full Text] [Related]
2. Clinical and hematologic aspects of the X-linked alpha-thalassemia/mental retardation syndrome (ATR-X).
Gibbons RJ; Brueton L; Buckle VJ; Burn J; Clayton-Smith J; Davison BC; Gardner RJ; Homfray T; Kearney L; Kingston HM
Am J Med Genet; 1995 Jan; 55(3):288-99. PubMed ID: 7726225
[TBL] [Abstract][Full Text] [Related]
3. X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: a new kindred with severe genital anomalies and mild hematologic expression.
McPherson EW; Clemens MM; Gibbons RJ; Higgs DR
Am J Med Genet; 1995 Jan; 55(3):302-6. PubMed ID: 7726227
[TBL] [Abstract][Full Text] [Related]
4. Male pseudohermaphroditism in sibs with the alpha-thalassemia/mental retardation (ATR-X) syndrome.
Reardon W; Gibbons RJ; Winter RM; Baraitser M
Am J Med Genet; 1995 Jan; 55(3):285-7. PubMed ID: 7726224
[TBL] [Abstract][Full Text] [Related]
5. X-linked alpha-thalassemia/mental retardation syndrome. Linkage analysis in a new family further supports localization in proximal Xq.
Houdayer CI; Toutain A; Ronce N; Lefort G; Sarda P; Taib J; Briault S; Lambert JC; Moraine CI
Ann Genet; 1993; 36(4):194-9. PubMed ID: 8166423
[TBL] [Abstract][Full Text] [Related]
6. Lumping Juberg-Marsidi syndrome and X-linked alpha-thalassemia/mental retardation syndrome?
Saugier-Veber P; Munnich A; Lyonnet S; Toutain A; Moraine C; Piussan C; Mathieu M; Gibbons RJ
Am J Med Genet; 1995 Jan; 55(3):300-1. PubMed ID: 7726226
[No Abstract] [Full Text] [Related]
7. [Alpha-thalassemia/mental retardation syndrome related to the X chromosome].
Lacombe D; Pedespan JM; Taib J; Micheau M; Guérin V
Arch Fr Pediatr; 1993 Oct; 50(8):723-4. PubMed ID: 8002754
[No Abstract] [Full Text] [Related]
8. [X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome].
Kurosawa K
Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):824-5. PubMed ID: 11529043
[No Abstract] [Full Text] [Related]
9. Germline and gonosomal mosaicism in the ATR-X syndrome.
Bachoo S; Gibbons RJ
Eur J Hum Genet; 1999 Dec; 7(8):933-6. PubMed ID: 10602370
[TBL] [Abstract][Full Text] [Related]
10. [Alpha thalassemia/metal retardation syndrome--a new X-chromosome linked recessive genetically inherited symptom complex].
Morava E; Kosztolányi G
Orv Hetil; 1996 Dec; 137(50):2799-801. PubMed ID: 9679615
[TBL] [Abstract][Full Text] [Related]
11. Molecular genetic study of japanese patients with X-linked alpha-thalassemia/mental retardation syndrome (ATR-X).
Wada T; Kubota T; Fukushima Y; Saitoh S
Am J Med Genet; 2000 Sep; 94(3):242-8. PubMed ID: 10995512
[TBL] [Abstract][Full Text] [Related]
12. Lujan-Fryns syndrome (X-linked mental retardation with marfanoid habitus): report of three cases and review.
Lacombe D; Bonneau D; Verloes A; Couet D; Koulischer L; Battin J
Genet Couns; 1993; 4(3):193-8. PubMed ID: 8267926
[TBL] [Abstract][Full Text] [Related]
13. Alpha thalassaemia mental retardation (ATR-X): an atypical family.
Logie LJ; Gibbons RJ; Higgs DR; Brown JK; Porteous ME
Arch Dis Child; 1994 May; 70(5):439-40. PubMed ID: 8017970
[TBL] [Abstract][Full Text] [Related]
14. FG syndrome: the trias mental retardation, hypotonia and constipation reviewed.
Zwamborn-Hanssen AM; Schrander-Stumpel CT; Smeets E; Decock P; Fryns JP
Genet Couns; 1995; 6(4):313-9. PubMed ID: 8775418
[TBL] [Abstract][Full Text] [Related]
15. [Chromosome X-linked mental retardation and marfanoid syndrome].
Fryns JP; Buttiens M; van den Berghe H
J Genet Hum; 1988 Jan; 36(1-2):123-8. PubMed ID: 3379374
[TBL] [Abstract][Full Text] [Related]
16. New X-linked syndrome with severe mental retardation, severely impaired vision, severe hearing defect, epileptic seizures, spasticity, restricted joint mobility, and early death.
Gustavson KH; Annerén G; Malmgren H; Dahl N; Ljunggren CG; Bäckman H
Am J Med Genet; 1993 Mar; 45(5):654-8. PubMed ID: 8456840
[TBL] [Abstract][Full Text] [Related]
17. [Alpha-thalassemia/mental retardation syndrome (ATR-X) in two brothers - clinical characteristics, diagnostics and genetic counselling issues].
Szczałuba K; Obersztyn E; Nowakowska B; Bernaciak J; Fisher C; Gibbons R; Mazurczak T; Bocian E
Med Wieku Rozwoj; 2011; 15(4):437-44. PubMed ID: 22516698
[TBL] [Abstract][Full Text] [Related]
18. [Coffin-Lowry syndrome. Description of a clinical case].
Venura A; Ferrari P; Benci E; Grando A
Pediatr Med Chir; 1988; 10(4):449-50. PubMed ID: 3231552
[TBL] [Abstract][Full Text] [Related]
19. Linkage analysis in three families with nonspecific X-linked mental retardation.
Claes S; Gu XX; Legius E; Lorenzetti E; Marynen P; Fryns JP; Cassiman JJ; Raeymaekers P
Am J Med Genet; 1996 Jul; 64(1):137-46. PubMed ID: 8826464
[TBL] [Abstract][Full Text] [Related]
20. Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?
Passos-Bueno MR; Byth BC; Rosenberg S; Takata RI; Bakker E; Beggs AH; Pavanello RC; Vainzof M; Davies KE; Zatz M
Am J Med Genet; 1993 Apr; 46(2):172-5. PubMed ID: 8484404
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
