247 related articles for article (PubMed ID: 3290491)
1. The Coffin-Lowry syndrome.
Young ID
J Med Genet; 1988 May; 25(5):344-8. PubMed ID: 3290491
[No Abstract] [Full Text] [Related]
2. The radiology of Coffin-Lowry syndrome.
Padley S; Hodgson SV; Sherwood T
Br J Radiol; 1990 Jan; 63(745):72-5. PubMed ID: 2306591
[No Abstract] [Full Text] [Related]
3. Hypopigmentation of the fundi associated with Pallister-Killian syndrome.
Birch M; Patterson A; Fryer A
J Pediatr Ophthalmol Strabismus; 1995; 32(2):128-31. PubMed ID: 7629670
[No Abstract] [Full Text] [Related]
4. [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]
5. Coffin-Lowry syndrome: a multicenter study.
Gilgenkrantz S; Mujica P; Gruet P; Tridon P; Schweitzer F; Nivelon-Chevallier A; Nivelon JL; Couillault G; David A; Verloes A
Clin Genet; 1988 Oct; 34(4):230-45. PubMed ID: 3069251
[TBL] [Abstract][Full Text] [Related]
6. Coffin-Lowry syndrome: clinical aspects at different ages and symptoms in female carriers.
Plomp AS; De Die-Smulders CE; Meinecke P; Ypma-Verhulst JM; Lissone DA; Fryns JP
Genet Couns; 1995; 6(3):259-68. PubMed ID: 8588856
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of Roberts syndrome.
Gruber A; Rabinerson D; Kaplan B; Ovadia Y
Prenat Diagn; 1994 Jun; 14(6):511-2. PubMed ID: 7524059
[No Abstract] [Full Text] [Related]
8. How wide is the clinical spectrum of the acrocallosal syndrome? Report of a mild case.
Turolla L; Clementi M; Tenconi R
J Med Genet; 1990 Aug; 27(8):516-8. PubMed ID: 2103730
[TBL] [Abstract][Full Text] [Related]
9. MRI of the hypophysis in a patient with the 18q- syndrome.
Bekiesiñska-Figatowska M; Walecki J
Neuroradiology; 2001 Oct; 43(10):875-6. PubMed ID: 11688707
[TBL] [Abstract][Full Text] [Related]
10. [Coffin-Lowry syndrome and hyperprolinemia].
Lacombe D; Parrot-Roulaud F; Castell JF; Serville F; Hehunstre JP; Battin J
Arch Fr Pediatr; 1993; 50(6):489-92. PubMed ID: 8135609
[TBL] [Abstract][Full Text] [Related]
11. Twins and their mildly affected mother with Weaver syndrome.
Dumić M; Vuković J; Cvitkovic M; Medica I
Clin Genet; 1993 Dec; 44(6):338-40. PubMed ID: 8131308
[TBL] [Abstract][Full Text] [Related]
12. The Miller-Dieker syndrome: a case report and review of the literature.
Izmeth MG; Parameshwar E
J Ment Defic Res; 1989 Jun; 33 ( Pt 3)():267-70. PubMed ID: 2666671
[TBL] [Abstract][Full Text] [Related]
13. A new X linked syndrome with mental retardation and craniofacial dysmorphism?
Hyde-Forster I; McCarthy G; Berry AC
J Med Genet; 1992 Oct; 29(10):736-8. PubMed ID: 1433236
[TBL] [Abstract][Full Text] [Related]
14. Retinal pigment mosaicism in Pallister-Killian syndrome (mosaic tetrasomy 12p).
Graham W; Brown SM; Shah F; Tonk VS; Kukolich MK
Arch Ophthalmol; 1999 Dec; 117(12):1648-9. PubMed ID: 10604674
[No Abstract] [Full Text] [Related]
15. Deletion of the short arm of chromosome 9. A clinically recognisable entity.
Fryns JP; Pedersen JC; Duyck H; Fabry G; Van den Berghe H
Eur J Pediatr; 1980 Sep; 134(3):201-4. PubMed ID: 7428770
[TBL] [Abstract][Full Text] [Related]
16. [Case imaging: 3. Dyke-Davidoff-Masson syndrome].
Caparrós Escudero C
Radiologia; 2007; 49(4):268; discussion 292. PubMed ID: 17594888
[No Abstract] [Full Text] [Related]
17. Diaphragmatic defects, craniofacial dysmorphism, cleft palate and distal limb deformities. - a new lethal syndrome.
Goddeeris P; Fryns JP; van den Berghe H
J Genet Hum; 1980 Mar; 28(1):57-60. PubMed ID: 7400786
[TBL] [Abstract][Full Text] [Related]
18. Deletion of chromosome 2 (p11-p13): case report and review.
Prasher VP; Krishnan VH; Clarke DJ; Maliszewska CT; Corbett JA
J Med Genet; 1993 Jul; 30(7):604-6. PubMed ID: 8411037
[TBL] [Abstract][Full Text] [Related]
19. [A new case of Weaver's syndrome observed in the neonatal period].
Di Comite A; Saracino P; Tonti R; De Vita L
Pediatria (Napoli); 1983; 91(4):435-9. PubMed ID: 6545407
[No Abstract] [Full Text] [Related]
20. Smith-Fineman-Myers syndrome: report of a third case.
Stephenson LD; Johnson JP
Am J Med Genet; 1985 Oct; 22(2):301-4. PubMed ID: 4050861
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
