187 related articles for article (PubMed ID: 8287182)
1. Congenital heart disease and Robinow syndrome.
Atalay S; Ege B; Imamoğlu A; Suskan E; Ocal B; Gümüş H
Clin Dysmorphol; 1993 Jul; 2(3):208-10. PubMed ID: 8287182
[TBL] [Abstract][Full Text] [Related]
2. Congenital heart disease and Robinow syndrome: coincidence or an additional component of the syndrome?
Webber SA; Wargowski DS; Chitayat D; Sandor GG
Am J Med Genet; 1990 Dec; 37(4):519-21. PubMed ID: 2260599
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Dwarfism, rhizomelic limb shortness, and abnormal face: new short stature syndrome sharing some manifestations with Robinow syndrome.
Turnpenny PD; Thwaites RJ
Am J Med Genet; 1992 Mar; 42(5):724-7. PubMed ID: 1632447
[TBL] [Abstract][Full Text] [Related]
5. Interstitial deletion 2q31 leads to q33.
Buchanan PD; Rhodes RL; Stevenson CE
Am J Med Genet; 1983 May; 15(1):121-6. PubMed ID: 6683075
[TBL] [Abstract][Full Text] [Related]
6. Velo-cardio-facial syndrome: a review of 120 patients.
Goldberg R; Motzkin B; Marion R; Scambler PJ; Shprintzen RJ
Am J Med Genet; 1993 Feb; 45(3):313-9. PubMed ID: 8434617
[TBL] [Abstract][Full Text] [Related]
7. Robinow syndrome.
Bhandari B; Tak SK; Gupta RS; Ramakrishnan S
Indian Pediatr; 1988 Aug; 25(8):784-6. PubMed ID: 3220568
[No Abstract] [Full Text] [Related]
8. [An unusual type of congenital heart disease associated with the Holt-Oram-syndrome (author's transl)].
Ruzić B; Bosnar B; Beleznay O
Radiologe; 1981 Jun; 21(6):296-9. PubMed ID: 7268028
[TBL] [Abstract][Full Text] [Related]
9. Unusual traits associated with Robinow syndrome.
Sabry MA; Ismail EA; al-Naggar RL; al-Torki NA; Farah S; al-Awadi SA; Obenbergerova D; Bastaki L
J Med Genet; 1997 Sep; 34(9):736-40. PubMed ID: 9321759
[TBL] [Abstract][Full Text] [Related]
10. The association between congenital heart disease and Down syndrome in prenatal life.
Paladini D; Tartaglione A; Agangi A; Teodoro A; Forleo F; Borghese A; Martinelli P
Ultrasound Obstet Gynecol; 2000 Feb; 15(2):104-8. PubMed ID: 10775990
[TBL] [Abstract][Full Text] [Related]
11. [Robinow syndrome].
Kawame H
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):236-7. PubMed ID: 11057211
[No Abstract] [Full Text] [Related]
12. Congenital heart defects in Aarskog syndrome.
Fernandez I; Tsukahara M; Mito H; Yoshii H; Uchida M; Matsuo K; Kajii T
Am J Med Genet; 1994 May; 50(4):318-22. PubMed ID: 8209909
[TBL] [Abstract][Full Text] [Related]
13. Autosomal recessive Robinow-like syndrome with anterior chamber cleavage anomalies.
Saal HM; Greenstein RM; Weinbaum PJ; Poole AE
Am J Med Genet; 1988 Jul; 30(3):709-18. PubMed ID: 3189394
[TBL] [Abstract][Full Text] [Related]
14. Robinow syndrome: with special emphasis on dermatoglyphics and hand malformations (split hand).
Balci S; Erçal MD; Say B; Atasü M
Clin Dysmorphol; 1993 Jul; 2(3):199-207. PubMed ID: 8287181
[TBL] [Abstract][Full Text] [Related]
15. Noncardiac malformations in congenital heart disease: a retrospective analysis of 305 pediatric autopsies.
Güçer S; Ince T; Kale G; Akçören Z; Ozkutlu S; Talim B; Cağlar M
Turk J Pediatr; 2005; 47(2):159-66. PubMed ID: 16052857
[TBL] [Abstract][Full Text] [Related]
16. [A liveborn child with complete triploidy].
Garty B; Mammon Z; Chemke M; Reisner S
Harefuah; 1985 Dec; 109(11):336-7. PubMed ID: 4093058
[No Abstract] [Full Text] [Related]
17. Anaesthetic implications of Robinow syndrome.
Lirk P; Rieder J; Schuerholz A; Keller C
Paediatr Anaesth; 2003 Oct; 13(8):725-7. PubMed ID: 14535914
[TBL] [Abstract][Full Text] [Related]
18. Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p.
Leichtman LG; Zackowski JL; Storto PD; Newlin A
Am J Med Genet; 1996 Jun; 63(3):434-7. PubMed ID: 8737648
[TBL] [Abstract][Full Text] [Related]
19. [Molecular diagnosis of CHARGE syndrom].
Pedersen AM; Skovby F
Ugeskr Laeger; 2007 Jan; 169(5):402-6. PubMed ID: 17280632
[TBL] [Abstract][Full Text] [Related]
20. Two cases of severe lethal Smith-Lemli-Opitz syndrome.
Belmont JW; Hawkins E; Hejtmancik JF; Greenberg F
Am J Med Genet; 1987 Jan; 26(1):65-7. PubMed ID: 3812579
[No Abstract] [Full Text] [Related]
[Next] [New Search]
