137 related articles for article (PubMed ID: 8465862)
1. Morfan: a new syndrome characterized by mental retardation, pre- and postnatal overgrowth, remarkable face and acanthosis nigricans in 5-year-old boy.
Seemanová E; Rüdiger HW; Dreyer M
Am J Med Genet; 1993 Feb; 45(4):525-8. PubMed ID: 8465862
[No Abstract] [Full Text] [Related]
2. MORFAN Syndrome: An Infantile Hypoinsulinemic Hypoketotic Hypoglycemia Due to an AKT2 Mutation.
Garg N; Bademci G; Foster J; Sıklar Z; Berberoglu M; Tekin M
J Pediatr; 2015 Aug; 167(2):489-91. PubMed ID: 26003998
[TBL] [Abstract][Full Text] [Related]
3. Rabson-Mendenhall syndrome.
Parveen BA; Sindhuja R
Int J Dermatol; 2008 Aug; 47(8):839-41. PubMed ID: 18717867
[TBL] [Abstract][Full Text] [Related]
4. Familial insulin resistant diabetes associated with acanthosis nigricans, polycystic ovaries, hypogonadism, pigmentary retinopathy, labyrinthine deafness, and mental retardation.
Boor R; Herwig J; Schrezenmeir J; Pontz BF; Schönberger W
Am J Med Genet; 1993 Mar; 45(5):649-53. PubMed ID: 8456839
[TBL] [Abstract][Full Text] [Related]
5. Weaver syndrome in two Japanese children.
Kondo I; Mori Y; Kuwajima K
Am J Med Genet; 1991 Nov; 41(2):221-4. PubMed ID: 1785638
[TBL] [Abstract][Full Text] [Related]
6. [Donohue's syndrome (Leprechaunism)].
Imamura T; Kobayashi M
Nihon Rinsho; 1994 Oct; 52(10):2643-7. PubMed ID: 7983792
[TBL] [Abstract][Full Text] [Related]
7. Two female siblings with a previously unreported MCA/MR syndrome: pre- and postnatal growth retardation, iris colobomata, spasticity, facial dysmorphism and dilated ventricles.
Yüksel A; Seven M; Deviren A; Söylemez MA; Hacihanefioğlu S; Ulutin T; Cenani A
Genet Couns; 1999; 10(3):265-9. PubMed ID: 10546098
[TBL] [Abstract][Full Text] [Related]
8. Brief clinical report: the Dubowitz syndrome in a teenager.
Fryns JP; Fabry G; Willemyns F; Van Den Berghe H
Am J Med Genet; 1979; 4(4):345-7. PubMed ID: 575467
[TBL] [Abstract][Full Text] [Related]
9. Short stature, psychomotor retardation, and unusual facial appearance in two brothers.
Smith RD; Fineman RM; Myers GG
Am J Med Genet; 1980; 7(1):5-9. PubMed ID: 7211953
[TBL] [Abstract][Full Text] [Related]
10. Report on two patients with Costello syndrome and sialuria.
Di Rocco M; Gatti R; Gandullia P; Barabino A; Picco P; Borrone C
Am J Med Genet; 1993 Nov; 47(7):1135-40. PubMed ID: 8291534
[TBL] [Abstract][Full Text] [Related]
11. Familial insulin resistance with acanthosis nigricans, acral hypertrophy, and muscle cramps.
Flier JS; Young JB; Landsberg L
N Engl J Med; 1980 Oct; 303(17):970-3. PubMed ID: 6997748
[No Abstract] [Full Text] [Related]
12. Cytogenetic abnormalities in two new patients with Pitt-Rogers-Danks phenotype.
Lindeman-Kusse MC; Van Haeringen A; Hoorweg-Nijman JJ; Brunner HG
Am J Med Genet; 1996 Dec; 66(1):104-12. PubMed ID: 8957526
[TBL] [Abstract][Full Text] [Related]
13. Trisomy 18 mosaicism in a mildly retarded boy with postnatal overgrowth.
Plessis G; Le Treust M; Lemaire F; Maugard T; Cau D
Ann Genet; 1997; 40(4):235-7. PubMed ID: 9526621
[TBL] [Abstract][Full Text] [Related]
14. A case of Morfan syndrome.
Hiscox B; Hu J; Young LC
Cutis; 2015 Mar; 95(3):E20-1. PubMed ID: 25844790
[No Abstract] [Full Text] [Related]
15. [Miescher's syndrome in siblings].
Ogawa A; Baba F
Nihon Shonika Gakkai Zasshi; 1969 Jun; 73(6):730-9. PubMed ID: 5817073
[No Abstract] [Full Text] [Related]
16. A further patient with the Pitt-Rogers-Danks syndrome of mental retardation, unusual face, and intrauterine growth retardation.
Donnai D
Am J Med Genet; 1986 May; 24(1):29-32. PubMed ID: 3706410
[TBL] [Abstract][Full Text] [Related]
17. Abnormal face, congenital absence of the left pericardium, mental retardation, and growth hormone deficiency.
Boscherini B; Galasso C; Bitti ML
Am J Med Genet; 1994 Jan; 49(1):111-3. PubMed ID: 8172237
[No Abstract] [Full Text] [Related]
18. [Simpson-Golabi-Behmel syndrome. A new overgrowth syndrome with increased risk of tumor development].
Weidle B; Orstavik KH
Tidsskr Nor Laegeforen; 1998 Apr; 118(10):1556-8. PubMed ID: 9615582
[TBL] [Abstract][Full Text] [Related]
19. Mild mental retardation with classic somatic phenotype in the Brachmann-de Lange syndrome.
Clericuzio CL
Am J Med Genet; 1993 Nov; 47(7):992-4. PubMed ID: 8291542
[TBL] [Abstract][Full Text] [Related]
20. Acanthosis Nigricans, insulin resistance (HOMA) and dyslipidemia among Native American children.
Copeland K; Pankratz K; Cathey V; Immohotichey P; Maddox J; Felton B; McIntosh R; Parker D; Burgin C; Blackett P
J Okla State Med Assoc; 2006 Jan; 99(1):19-24. PubMed ID: 16499154
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
