159 related articles for article (PubMed ID: 7573157)
1. Identical twins with Cohen syndrome.
North KN; Fulton AB; Whiteman DA
Am J Med Genet; 1995 Jul; 58(1):54-8. PubMed ID: 7573157
[TBL] [Abstract][Full Text] [Related]
2. [Cohen's syndrome in 2 sisters].
Doyard P; Mattei JF
Sem Hop; 1984 Apr; 60(16):1143-7. PubMed ID: 6326307
[TBL] [Abstract][Full Text] [Related]
3. Phenotypic discordance in monozygotic twins with 22q11.2 deletion.
Yamagishi H; Ishii C; Maeda J; Kojima Y; Matsuoka R; Kimura M; Takao A; Momma K; Matsuo N
Am J Med Genet; 1998 Jul; 78(4):319-21. PubMed ID: 9714432
[TBL] [Abstract][Full Text] [Related]
4. Cohen syndrome: further delineation and inheritance.
Kousseff BG
Am J Med Genet; 1981; 9(1):25-30. PubMed ID: 7246618
[TBL] [Abstract][Full Text] [Related]
5. [Monozygotic twins with Williams-Beuren or 'elfen-face' syndrome].
Oorthuys JW
Tijdschr Kindergeneeskd; 1984 Oct; 52(5):197-200. PubMed ID: 6542697
[TBL] [Abstract][Full Text] [Related]
6. Coats-type retinal telangiectasia in case of Kabuki make-up syndrome (Niikawa-Kuroki syndrome).
Anandan M; Porter NJ; Nemeth AH; Blair E; Downes SM
Ophthalmic Genet; 2005 Dec; 26(4):181-3. PubMed ID: 16352479
[TBL] [Abstract][Full Text] [Related]
7. [Cohen syndrome. Description of a new case and study of the central nervous system using nuclear magnetic resonance].
Gabrielli O; Pierleoni C; Barbato M; Bonifazi V; Oggiano N; Carlucci A
Minerva Pediatr; 1989 Dec; 41(12):615-8. PubMed ID: 2699519
[TBL] [Abstract][Full Text] [Related]
8. The Cohen syndrome: does mottled retina separate a Finnish and a Jewish type?
Kondo I; Nagataki S; Miyagi N
Am J Med Genet; 1990 Sep; 37(1):109-13. PubMed ID: 2240027
[TBL] [Abstract][Full Text] [Related]
9. [The Cohen syndrome].
Dumić M; Ille J; Cvitković M; Kordić R
Lijec Vjesn; 1996 Sep; 118(9):202-4. PubMed ID: 9011740
[TBL] [Abstract][Full Text] [Related]
10. [Cohen syndrome: report of two cases in female twins].
Arcas Martínez J; García Peñas JJ; Ramos Lizana J; Díaz González C; Pascual Castroviejo I
An Esp Pediatr; 1991 Jan; 34(1):83-5. PubMed ID: 2018266
[No Abstract] [Full Text] [Related]
11. The Cohen syndrome: report of a case.
Naritomi K; Chinen Y
Jpn J Hum Genet; 1997 Sep; 42(3):457-9. PubMed ID: 12503195
[TBL] [Abstract][Full Text] [Related]
12. New autosomal-recessive syndrome of Leber congenital amaurosis, short stature, growth hormone insufficiency, mental retardation, hepatic dysfunction, and metabolic acidosis.
Ehara H; Nakano C; Ohno K; Goto YI; Takeshita K
Am J Med Genet; 1997 Aug; 71(3):258-66. PubMed ID: 9268092
[TBL] [Abstract][Full Text] [Related]
13. Tapetoretinal degeneration in brothers with apparent Cohen syndrome: nosology with Mirhosseini-Holmes-Walton syndrome.
Steinlein O; Tariverdian G; Boll HU; Vogel F
Am J Med Genet; 1991 Nov; 41(2):196-200. PubMed ID: 1785634
[TBL] [Abstract][Full Text] [Related]
14. The Cohen syndrome: report of five new cases and a review of the literature.
Friedman E; Sack J
J Craniofac Genet Dev Biol; 1982; 2(3):193-200. PubMed ID: 7166592
[TBL] [Abstract][Full Text] [Related]
15. [Cohen syndrome. A new case and review of the literature].
Calzolari S; Ballardini M; De Marco P
Minerva Pediatr; 1995 Mar; 47(3):83-7. PubMed ID: 7791717
[TBL] [Abstract][Full Text] [Related]
16. [Cohen syndrome in 2 brothers].
Zetler S; Römke C; Aksu F
Klin Padiatr; 1987; 199(1):55-7. PubMed ID: 3560767
[TBL] [Abstract][Full Text] [Related]
17. The Cohen syndrome.
Fryns JP; Van den Berghe H
J Genet Hum; 1981 Dec; 29(4):449-53. PubMed ID: 7328419
[TBL] [Abstract][Full Text] [Related]
18. [Hereditary syndromes featuring oligophrenia and obesity].
Ustinova EV
Zh Nevropatol Psikhiatr Im S S Korsakova; 1981; 81(3):435-9. PubMed ID: 7020300
[No Abstract] [Full Text] [Related]
19. New syndrome: mixed hearing loss, mental deficiency, growth retardation, short clubbed digits, and EEG abnormalities in monozygous female twins.
Pfeiffer RA
Am J Med Genet; 1987 Jul; 27(3):639-44. PubMed ID: 3631135
[No Abstract] [Full Text] [Related]
20. Six additional cases of the KBG syndrome: clinical reports and outline of the diagnostic criteria.
Zollino M; Battaglia A; D'Avanzo MG; Della Bruna MM; Marini R; Scarano G; Cappa M; Neri G
Am J Med Genet; 1994 Sep; 52(3):302-7. PubMed ID: 7810561
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]