85 related articles for article (PubMed ID: 2274440)
1. [Silver-Russell syndrome. Presentation of a case with autosomal dominant heredity].
Zanchetta S; Praderio R; Marcer G; Bagnani A
Pediatr Med Chir; 1990; 12(3):277-9. PubMed ID: 2274440
[TBL] [Abstract][Full Text] [Related]
2. Autosomal dominant Russell-Silver syndrome.
Al-Fifi S; Teebi AS; Shevell M
Am J Med Genet; 1996 Jan; 61(1):96-7. PubMed ID: 8741931
[No Abstract] [Full Text] [Related]
3. Distinctive autosomal or X-linked dominant syndrome of microcephaly, mild developmental delay, short stature, and distinctive face.
Winter RM
Am J Med Genet; 1993 Nov; 47(6):917-20. PubMed ID: 7506485
[TBL] [Abstract][Full Text] [Related]
4. Cataracts, aberrant oral frenula, and growth retardation: a new autosomal dominant syndrome.
Wellesley D; Carman P; French N; Goldblatt J
Am J Med Genet; 1991 Sep; 40(3):341-2. PubMed ID: 1951441
[TBL] [Abstract][Full Text] [Related]
5. Pitt-Rogers-Danks syndrome: further delineation.
Lizcano-Gil LA; García-Cruz D; García-Cruz O; Sánchez-Corona J
Am J Med Genet; 1995 Feb; 55(4):420-2. PubMed ID: 7762580
[TBL] [Abstract][Full Text] [Related]
6. Autosomal dominant inheritance of the Kabuki make-up (Niikawa-Kuroki) syndrome.
Halal F; Gledhill R; Dudkiewicz A
Am J Med Genet; 1989 Jul; 33(3):376-81. PubMed ID: 2801772
[TBL] [Abstract][Full Text] [Related]
7. A rare cause of short stature: Leri Weill dyschondrosteosis.
Cakir M; Kalyoncu M; Odemiş E; Okten A
Genet Couns; 2003; 14(2):215-20. PubMed ID: 12872816
[TBL] [Abstract][Full Text] [Related]
8. Familial Brachmann-de Lange syndrome: further evidence for autosomal dominant inheritance and review of the literature.
Feingold M; Lin AE
Am J Med Genet; 1993 Nov; 47(7):1064-7. PubMed ID: 8291524
[TBL] [Abstract][Full Text] [Related]
9. Surgical closure of an atrial septal defect in an 11-year-old girl with Silver-Russell syndrome.
Vahlas CE; Chatzis AC; Giannopoulos NM; Contrafouris CA; Milonakis MC; Sarris GE
J Cardiovasc Med (Hagerstown); 2007 Oct; 8(10):850-1. PubMed ID: 17885526
[TBL] [Abstract][Full Text] [Related]
10. Johnson-McMillin syndrome: report of another family.
Hennekam RC; Holtus FJ
Am J Med Genet; 1993 Oct; 47(5):714-6. PubMed ID: 8267002
[TBL] [Abstract][Full Text] [Related]
11. Male-to-male transmission of mild Brachmann-de Lange syndrome.
Chodirker BN; Chudley AE
Am J Med Genet; 1994 Sep; 52(3):331-3. PubMed ID: 7528973
[TBL] [Abstract][Full Text] [Related]
12. Further delineation of the ear, patella, short stature syndrome (Meier-Gorlin syndrome).
Boles RG; Teebi AS; Schwartz D; Harper JF
Clin Dysmorphol; 1994 Jul; 3(3):207-14. PubMed ID: 7981855
[TBL] [Abstract][Full Text] [Related]
13. [Low levels of somatomedin C and short stature in the Silver-Russell syndrome].
Di Pietro A; Proverbio MR; D'Avolio G; Coletta M; Tammaro V
Pediatr Med Chir; 1994; 16(2):153-4. PubMed ID: 8078790
[TBL] [Abstract][Full Text] [Related]
14. Monozygotic twins discordant for the Russell-Silver syndrome.
Bailey W; Popovich B; Jones KL
Am J Med Genet; 1995 Aug; 58(2):101-5. PubMed ID: 8533797
[TBL] [Abstract][Full Text] [Related]
15. Autosomal dominant partial lipodystrophy associated with Rieger anomaly, short stature, and insulinopenic diabetes.
Aarskog D; Ose L; Pande H; Eide N
Am J Med Genet; 1983 May; 15(1):29-38. PubMed ID: 6407320
[TBL] [Abstract][Full Text] [Related]
16. Silver-Russell syndrome and its genetic origins.
Rossignol S
J Endocrinol Invest; 2006; 29(1 Suppl):9-10. PubMed ID: 16615300
[TBL] [Abstract][Full Text] [Related]
17. New syndrome: familial proportionate short stature, intrauterine growth retardation, and recurrent locking of the fingers.
Eng CE; Strom CM
Am J Med Genet; 1987 Jan; 26(1):217-20. PubMed ID: 3812565
[No Abstract] [Full Text] [Related]
18. Niikawa-Kuroki syndrome.
Roccella M
Minerva Pediatr; 1999; 51(7-8):271-8. PubMed ID: 10634060
[TBL] [Abstract][Full Text] [Related]
19. Epigenetics in Silver-Russell syndrome.
Rossignol S; Netchine I; Le Bouc Y; Gicquel C
Best Pract Res Clin Endocrinol Metab; 2008 Jun; 22(3):403-14. PubMed ID: 18538282
[TBL] [Abstract][Full Text] [Related]
20. [Silver-Russell syndrome. A possible example of genetic heterogenicity].
Giuffrè L; Benigno V; Cammarata M; Corsello G; Piccione M; Vitaliti SM
Minerva Pediatr; 1986 Oct; 38(19):849-53. PubMed ID: 3025578
[No Abstract] [Full Text] [Related]
[Next] [New Search]
