These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
119 related articles for article (PubMed ID: 4399309)
1. [Presentation of a case of an unusual malformative syndrome: the Schönenberg syndrome]. Buffoni L; Chiossi FM Minerva Pediatr; 1971 Sep; 23(38):1549-54. PubMed ID: 4399309 [No Abstract] [Full Text] [Related]
3. [Skeletal changes in a case of unusual chromosome aberration. (Patient with chromosome complex 48, XXXX-49, XXXXX: comparison with the syndrome 49,XXXXY]. Dallapiccola B; Pistocchi GF Radiol Med; 1968 Aug; 54(8):737-50. PubMed ID: 5190487 [No Abstract] [Full Text] [Related]
4. [Endocrinologic study of 4 children with Noonan's syndrome]. Carratù A; Pasquino A; Randone G; Boscherini B Minerva Pediatr; 1975 May; 27(17):1020-4. PubMed ID: 237229 [No Abstract] [Full Text] [Related]
5. [Phenotypic and cytogenetic analysis of an unusual malformative syndrome (trisomy 9 p+)]. Chipail A; Constantinescu V; Covic M; Angheloni T Rev Pediatr Obstet Ginecol Pediatr; 1976; 25(3):201-10. PubMed ID: 11544 [No Abstract] [Full Text] [Related]
6. [On a case of malformative syndrome with trisomy D 13-15]. Cattarozzi G; Scarpa P Minerva Pediatr; 1967 Nov; 19(47):2098-9. PubMed ID: 4974489 [No Abstract] [Full Text] [Related]
7. Pre- and postnatal growth retardation with severe mental retardation, acral limb deficiencies and ocular anomalies: a new syndrome of inherited intrauterine dwarfism? Fryns JP; van den Berghe H Acta Paediatr Belg; 1977; 30(4):227-32. PubMed ID: 417557 [No Abstract] [Full Text] [Related]
10. A new Seckel-like syndrome of primordial dwarfism. Buebel MS; Salinas CF; Pai GS; Macpherson RI; Greer MK; Perez-Comas A Am J Med Genet; 1996 Aug; 64(3):447-52. PubMed ID: 8862620 [TBL] [Abstract][Full Text] [Related]
12. [Multiple congenital malformations in a boy with a chromosome abnormality of the group F (46-XY, 20-P), the son of a clinically healthy subject with an analogous chromosome malformation]. Loiodice G; Rovetta DG; Bellicini G; Callura G; Bergamo F Minerva Pediatr; 1970 May; 22(21):1084-8. PubMed ID: 4394837 [No Abstract] [Full Text] [Related]
13. A new syndrome. Short limbs, abnormal facial appearance, and congenital heart defect. Barrow M; Fitzsimmons JS Am J Med Genet; 1984 Jul; 18(3):431-3. PubMed ID: 6476004 [No Abstract] [Full Text] [Related]
14. Radial ray defects, triangular face, telecanthus, sparse hair, dwarfism, and mental retardation. Imaizumi K; Kuroki Y Am J Med Genet; 1991 Nov; 41(2):162-3. PubMed ID: 1785626 [No Abstract] [Full Text] [Related]
18. [The Rubinstein-Taybi syndrome]. Predescu V; Oancea C; Stefan M; Christodorescu D Neurol Psihiatr Neurochir; 1971; 16(2):101-7. PubMed ID: 5578348 [No Abstract] [Full Text] [Related]
19. [Cryptorchidism with didymo-epididymal dissociation and Robinow's syndrome: 2 case reports]. Fabbro MA; D'Agostino S; Costa L; Musi L; Cappellari F Pediatr Med Chir; 1997; 19(2):121-4. PubMed ID: 9312747 [TBL] [Abstract][Full Text] [Related]
20. The association of spinal retroflexion with limb anomalies. Bowden RA; Stephens TD; Lemire RJ Teratology; 1980 Feb; 21(1):53-9. PubMed ID: 6247773 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]