69 related articles for article (PubMed ID: 6686981)
1. Silver syndrome: an infant with necropsy findings.
Imaizumi K; Ogino T; Kajii T
Jinrui Idengaku Zasshi; 1983 Sep; 28(3):231-4. PubMed ID: 6686981
[No Abstract] [Full Text] [Related]
2. [Weaver syndrome. Apropos of a case].
Alvarez-Coca J; Fullana A; Morena V; Gonzalez M; Oliver A; Gracia R; Peralta A
An Esp Pediatr; 1984 Oct; 21(6):626-8. PubMed ID: 6524773
[No Abstract] [Full Text] [Related]
3. 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]
4. [Silver-Russel Syndrome in aa 13-month old girl].
Hajdas-Kudela I; Jamroz E; Marszał E
Pol Merkur Lekarski; 1997 Jun; 2(12):387-8. PubMed ID: 9424332
[TBL] [Abstract][Full Text] [Related]
5. An infant with 45 chromosomes including a D-E (13-15-17-18) translocation chromosome.
Borgaonkar DS; Mules E; Scott CI
Johns Hopkins Med J; 1971 May; 128(5):282-8. PubMed ID: 5556542
[No Abstract] [Full Text] [Related]
6. Perinatal imaging findings of Galloway-Mowat syndrome.
Chen CP; Lin SP; Tsai JD; Huang JK; Yen JL; Tseng CC; Wang W
Genet Couns; 2007; 18(3):353-5. PubMed ID: 18019379
[No Abstract] [Full Text] [Related]
7. Monozygotic twins discordant for the Russell-Silver syndrome.
Samn M; Lewis K; Blumberg B
Am J Med Genet; 1990 Dec; 37(4):543-5. PubMed ID: 2260605
[TBL] [Abstract][Full Text] [Related]
8. [Genetic-morphologic fatal syndromes. Fetal akinesia sequence (Pena-Shokeir syndrome I)].
Henkel KE; Pfeiffer RA; Stöss H
Pathologe; 1993 Jul; 14(4):216-8. PubMed ID: 8367387
[No Abstract] [Full Text] [Related]
9. Fryns syndrome: an autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia.
Cunniff C; Jones KL; Saal HM; Stern HJ
Pediatrics; 1990 Apr; 85(4):499-504. PubMed ID: 2314962
[TBL] [Abstract][Full Text] [Related]
10. [Genetic-morphologic fatal syndromes. Cerebro-oculo-facioskeletal syndrome (Pena-Shokeir syndrome II)].
Henkel KE; Pfeiffer RA; Stöss H
Pathologe; 1993 Jul; 14(4):219-20. PubMed ID: 8367388
[No Abstract] [Full Text] [Related]
11. [Genetic morphologic fatal syndromes. Neu-Laxova syndrome].
Henkel KE; Pfeiffer RA; Stöss H
Pathologe; 1993 Sep; 14(5):271-3. PubMed ID: 8415438
[No Abstract] [Full Text] [Related]
12. [Brachmann-de Lange syndrome: report of 4 cases in Mexican children].
Villegas-Camargo I; Lacro RV; Lyons-Jones K
Bol Med Hosp Infant Mex; 1987 Dec; 44(12):766-70. PubMed ID: 3426781
[No Abstract] [Full Text] [Related]
13. The Pena-Shokeir syndrome: report of nine Dutch cases.
Lindhout D; Hageman G; Beemer FA; Ippel PF; Breslau-Siderius L; Willemse J
Am J Med Genet; 1985 Aug; 21(4):655-68. PubMed ID: 3895932
[TBL] [Abstract][Full Text] [Related]
14. Distal obstructive uropathy with polydactyly: a new syndrome?
Halal F
Am J Med Genet; 1986 Aug; 24(4):753-7. PubMed ID: 3740105
[No Abstract] [Full Text] [Related]
15. [Chorangioma of the placenta].
Ulrich B; Heidenreich W; Borgmann U
Z Geburtshilfe Neonatol; 1999; 203(4):173-5. PubMed ID: 10483701
[TBL] [Abstract][Full Text] [Related]
16. Yunis-Varon syndrome.
Bhatia S; Holla RG
Indian Pediatr; 2005 Apr; 42(4):373-5. PubMed ID: 15876600
[TBL] [Abstract][Full Text] [Related]
17. Guadalajara camptodactyly syndrome. A distinct probably autosomal recessive disorder.
Cantú JM; Rivera H; Nazará Z; Rojas Q; Hernández A; García-Cruz D
Clin Genet; 1980 Sep; 18(3):153-9. PubMed ID: 7192193
[TBL] [Abstract][Full Text] [Related]
18. The Coffin-Siris syndrome: a case report.
Ueda K; Saito A; Nakano H; Iinuma K
Helv Paediatr Acta; 1980 Sep; 35(4):385-90. PubMed ID: 7192700
[TBL] [Abstract][Full Text] [Related]
19. Six patients with oral-facial-digital syndrome IV: the case for heterogeneity.
Toriello HV; Carey JC; Suslak E; Desposito FR; Leonard B; Lipson M; Friedman BD; Hoyme HE
Am J Med Genet; 1997 Mar; 69(3):250-60. PubMed ID: 9096753
[TBL] [Abstract][Full Text] [Related]
20. [The oro-facial-digital syndrome. Symptoms and prognosis].
Majewski F; Lenz W; Pfeiffer RA; Tünte W; Müller H
Z Kinderheilkd; 1972; 112(1):89-112. PubMed ID: 4336265
[No Abstract] [Full Text] [Related]
[Next] [New Search]