141 related articles for article (PubMed ID: 3582410)
1. Sagittal craniostenosis, congenital heart disease, mental deficiency and various dysmorphies in two sibs--a "new" syndrome?
Pfeiffer RA; Singer H; Zschiesche S
Eur J Pediatr; 1987 Jan; 146(1):75-8. PubMed ID: 3582410
[TBL] [Abstract][Full Text] [Related]
2. An unusual, possibly "new" MA/MR syndrome with sagittal craniosynostosis.
Pfeiffer RA; Tietze U; Welte W
Eur J Pediatr; 1987 Jan; 146(1):74-5. PubMed ID: 3034618
[TBL] [Abstract][Full Text] [Related]
3. Pfeiffer type cardiocranial syndrome: a third case report.
Williamson-Kruse L; Biesecker LG
J Med Genet; 1995 Nov; 32(11):901-3. PubMed ID: 8592338
[TBL] [Abstract][Full Text] [Related]
4. Studies of malformation syndromes of man XXXIX: a craniosynostosis-craniofacial dysostosis syndrome with mental retardation and other malformations: "craniofacial dyssynostosis".
Neuhäuser G; Kaveggia EG; Opitz JM
Eur J Pediatr; 1976 Aug; 123(1):15-28. PubMed ID: 954768
[TBL] [Abstract][Full Text] [Related]
5. Unusual association of congenital malformations: craniosynostosis, heart defect, abnormal intestinal innervation and urogenital abnormalities.
Van Nesselrooij BP; Spliet W; Beemer FA
Clin Dysmorphol; 1998 Jan; 7(1):51-3. PubMed ID: 9546831
[TBL] [Abstract][Full Text] [Related]
6. Skeletal anomalies in genetically determined congenital heart disease.
Poznanski AK; Stern AM; Gall JC
Radiol Clin North Am; 1971 Dec; 9(3):435-58. PubMed ID: 5145748
[No Abstract] [Full Text] [Related]
7. Intrafamilial variability of Pfeiffer-type cardiocranial syndrome.
Digilio MC; Marino B; Borzaga U; Giannotti A; Dallapiccola B
Am J Med Genet; 1997 Dec; 73(4):480-3. PubMed ID: 9415478
[TBL] [Abstract][Full Text] [Related]
8. A new recognisable syndrome in three sibs with congenital heart disease, round face with depressed nasal bridge, short stature, and developmental retardation.
Sonoda T; Ohdo S; Madokoro H; Ohba K
J Med Genet; 1988 Oct; 25(10):711-3. PubMed ID: 3225826
[TBL] [Abstract][Full Text] [Related]
9. Unknown syndrome in sibs: microcephaly, seizures, mental retardation, congenital heart disease, and skeletal abnormalities.
Holmes GE; Schimke RN
J Med Genet; 1989 Oct; 26(10):665-6. PubMed ID: 2585466
[TBL] [Abstract][Full Text] [Related]
10. Sagittal craniosynostosis, Dandy-Walker malformation, and hydrocephalus: a unique multiple malformation syndrome.
Braddock SR; Jones KL; Superneau DW; Jones MC
Am J Med Genet; 1993 Oct; 47(5):640-3; discussion 644. PubMed ID: 8266990
[TBL] [Abstract][Full Text] [Related]
11. Limb abnormalities and mental retardation.
Smith GF; Schindeler J; Elbualy S; Shear C
J Ment Defic Res; 1970 Dec; 14(4):319-41. PubMed ID: 5517969
[No Abstract] [Full Text] [Related]
12. Craniosynostosis and congenital heart anomalies associated with a maternal deletion of 15q15-22.1.
Shur N; Cowan J; Wheeler PG
Am J Med Genet A; 2003 Aug; 120A(4):542-6. PubMed ID: 12884436
[TBL] [Abstract][Full Text] [Related]
13. Further delineation of the Baller-Gerold syndrome.
Lin AE; McPherson E; Nwokoro NA; Clemens M; Losken HW; Mulvihill JJ
Am J Med Genet; 1993 Feb; 45(4):519-24. PubMed ID: 8465861
[TBL] [Abstract][Full Text] [Related]
14. Ethical challenges in infant heart transplantation: a clinical case presentation.
Johnston JK; Orr RD
J Transpl Coord; 1999 Dec; 9(4):263-5. PubMed ID: 10889700
[TBL] [Abstract][Full Text] [Related]
15. [Carpenter's syndrome].
Piussan C; Van Poperinghe M; Grumbach Y; Audebert M; Helsemans C; Risbourg B
Arch Fr Pediatr; 1977 Nov; 34(9):891-8. PubMed ID: 606189
[TBL] [Abstract][Full Text] [Related]
16. Mowat-Wilson syndrome with craniosynostosis: a case report.
Adam MP; Justice AN; Bean LJ; Fernhoff PM
Am J Med Genet A; 2008 Jan; 146A(2):245-6. PubMed ID: 18076118
[No Abstract] [Full Text] [Related]
17. [Study of extracardiac malformation and anomalies of dermatoglyphics in a group of patients with congenital heart diseases].
Burguet W; Collard P; Jovanovic M
Acta Cardiol; 1970; 25(3):291-302. PubMed ID: 4247371
[No Abstract] [Full Text] [Related]
18. Parental consanguinity in the blepharophimosis, heart defect, hypothyroidism, mental retardation syndrome (Young-Simpson syndrome).
Bonthron DT; Barlow KM; Burt AM; Barr DG
J Med Genet; 1993 Mar; 30(3):255-6. PubMed ID: 8474111
[TBL] [Abstract][Full Text] [Related]
19. Baller-Gerold syndrome: case report and clinical and radiological review.
Dallapiccola B; Zelante L; Mingarelli R; Pellegrino M; Bertozzi V
Am J Med Genet; 1992 Feb; 42(3):365-8. PubMed ID: 1536180
[TBL] [Abstract][Full Text] [Related]
20. Marfanoid features and craniosynostosis: report of one case and review.
Lacombe D; Battin J
Clin Dysmorphol; 1993 Jul; 2(3):220-4. PubMed ID: 8287183
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]