187 related articles for article (PubMed ID: 6258433)
1. The Dubowitz syndrome: further observations.
Orrison WW; Schnitzler ER; Chun RW
Am J Med Genet; 1980; 7(2):155-70. PubMed ID: 6258433
[TBL] [Abstract][Full Text] [Related]
2. Filippi syndrome: report of three additional cases.
Williams MS; Williams JL; Wargowski DS; Pauli RM; Pletcher BA
Am J Med Genet; 1999 Nov; 87(2):128-33. PubMed ID: 10533026
[TBL] [Abstract][Full Text] [Related]
3. The Dubowitz syndrome.
Wilroy RS; Tipton RE; Summitt RL
Am J Med Genet; 1978; 2(3):275-84. PubMed ID: 263660
[TBL] [Abstract][Full Text] [Related]
4. [Dubowitz syndrome. A diagnosis not to be missed].
Mathieu M; Berquin P; Epelbaum S; Lenaerts C; Piussan C
Arch Fr Pediatr; 1991 Dec; 48(10):715-8. PubMed ID: 1793348
[TBL] [Abstract][Full Text] [Related]
5. The Dubowitz syndrome: the psychological status of ten cases at follow-up.
Parrish JM; Wilroy RS
Am J Med Genet; 1980; 6(1):3-8. PubMed ID: 7190357
[TBL] [Abstract][Full Text] [Related]
6. Dubowitz syndrome: review of 141 cases including 36 previously unreported patients.
Tsukahara M; Opitz JM
Am J Med Genet; 1996 May; 63(1):277-89. PubMed ID: 8723121
[TBL] [Abstract][Full Text] [Related]
7. Floating-Harbor syndrome in a Kuwaiti patient: a case report and literature review.
Bastaki L; El-Nabi MM; Azab AS; Gouda SA; Al-Wadaani AM; Naguib KK
East Mediterr Health J; 2007; 13(4):975-9. PubMed ID: 17955782
[No Abstract] [Full Text] [Related]
8. Short stature, microcephaly, characteristic face, syndactyly and mental retardation: the Filippi syndrome. Report on a second family.
Meinecke P
Genet Couns; 1993; 4(2):147-51. PubMed ID: 8395190
[TBL] [Abstract][Full Text] [Related]
9. Dubowitz syndrome: a defect in the cholesterol biosynthetic pathway?
Ahmad A; Amalfitano A; Chen YT; Kishnani PS; Miller C; Kelley R
Am J Med Genet; 1999 Oct; 86(5):503-4. PubMed ID: 10508998
[No Abstract] [Full Text] [Related]
10. The Dubowitz syndrome--one more case.
Chrzanowska KH; Krajewska-Walasek M
Klin Padiatr; 1987; 199(5):370-2. PubMed ID: 3316825
[TBL] [Abstract][Full Text] [Related]
11. Mild growth retardation and developmental delay, microcephaly, and a distinctive facial appearance.
Partington M; Anderson D
Am J Med Genet; 1994 Jan; 49(2):247-50. PubMed ID: 7509568
[TBL] [Abstract][Full Text] [Related]
12. Dubowitz syndrome: long-term follow-up of an original patient.
Hansen KE; Kirkpatrick SJ; Laxova R
Am J Med Genet; 1995 Jan; 55(2):161-4. PubMed ID: 7536394
[TBL] [Abstract][Full Text] [Related]
13. The Dubowitz syndrome: a retrospective.
Moller KT; Gorlin RJ
J Craniofac Genet Dev Biol Suppl; 1985; 1():283-6. PubMed ID: 3877102
[TBL] [Abstract][Full Text] [Related]
14. Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome?
Filippi G
Am J Med Genet; 1985 Dec; 22(4):821-4. PubMed ID: 4073130
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Craniodigital syndromes: report of a child with Filippi syndrome and discussion of differential diagnosis.
Toriello HV; Higgins JV
Am J Med Genet; 1995 Jan; 55(2):200-4. PubMed ID: 7717418
[TBL] [Abstract][Full Text] [Related]
18. [The Dubowitz syndrome].
Dumić M; Cvitković M; Letinić D; Filipović-Grcić B; Kordić R
Lijec Vjesn; 1994; 116(5-6):135-7. PubMed ID: 7968200
[TBL] [Abstract][Full Text] [Related]
19. Dubowitz syndrome.
Wilhelm OL; Méhes K
Acta Paediatr Hung; 1986; 27(1):67-75. PubMed ID: 3730185
[TBL] [Abstract][Full Text] [Related]
20. Pitt-Rogers-Danks syndrome: the result of a 4p microdeletion.
Clemens M; Martsolf JT; Rogers JG; Mowery-Rushton P; Surti U; McPherson E
Am J Med Genet; 1996 Dec; 66(1):95-100. PubMed ID: 8957524
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]