75 related articles for article (PubMed ID: 15521104)
1. Hypotriploidy 68,XX: a new case report and review of earlier cases.
Hoedemaekers YM; De Kleine MJ; Stevens-Kroef MJ; Smeets EE; Schrander-Stumpel CT
Genet Couns; 2004; 15(3):329-33. PubMed ID: 15521104
[TBL] [Abstract][Full Text] [Related]
2. The bicuspid aortic valve--an autopsy study.
Deshpande J; Kinare SG
Indian J Pathol Microbiol; 1991 Apr; 34(2):112-8. PubMed ID: 1752636
[TBL] [Abstract][Full Text] [Related]
3. A new case of a severe clinical phenotype of the cat-eye syndrome.
Denavit TM; Malan V; Grillon C; Sanlaville D; Ardalan A; Jacquemont ML; Burglen L; Taillemite JL; Portnoi MF
Genet Couns; 2004; 15(4):443-8. PubMed ID: 15658620
[TBL] [Abstract][Full Text] [Related]
4. 49, XXXXY syndrome with severe vesico-ureteral reflux and hydronephrosis: report of one case.
Chang JT; Chiu PC; Chen YY; Chao MC; Hsieh KS
Acta Paediatr Taiwan; 2005; 46(1):35-8. PubMed ID: 16302576
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. [Triploidy in newborn infants].
Küster W; Beckmann H; Gebauer HJ; Majewski F
Monatsschr Kinderheilkd; 1988 Apr; 136(4):210-3. PubMed ID: 2838747
[TBL] [Abstract][Full Text] [Related]
7. Bilateral microtia with severe cardiac defect: a new syndrome, or a severe manifestation of the oculoauriculovertebral spectrum?
McKee S; Mabrouk R; Bali S
Clin Dysmorphol; 2006 Apr; 15(2):121-2. PubMed ID: 16531742
[TBL] [Abstract][Full Text] [Related]
8. [Postnatal diagnosis and prognosis of 2 cases of triploidy].
Ben Hamouda H; Tfifha M; Elghezal H; Tlili Y; Soua H; Saad A; Sfar MT
Arch Pediatr; 2010 Jul; 17(7):1078-82. PubMed ID: 20444585
[TBL] [Abstract][Full Text] [Related]
9. Asphyxiating thoracic dystrophy and syndactyly of the toes in a newborn: coincidence or a new association?
Tastekin A; Polat P; Ors R
Genet Couns; 2003; 14(1):113-4. PubMed ID: 12725597
[No Abstract] [Full Text] [Related]
10. Duplication of (12)(pter-q13.3) combined with deletion of (22)(pter-q11.2) in a patient with features of both chromosome aberrations.
Tyshchenko NA; Riegel M; Evseenkova EG; Zerova TE; Gorovenko NG; Schinzel A
Eur J Med Genet; 2007; 50(2):128-32. PubMed ID: 17174617
[TBL] [Abstract][Full Text] [Related]
11. MURCS Association: a rare association with patent ductus arteriosus and bicuspid aortic valve.
Ramakrishna ; Kotecha N; Patel CA; Pipavat R
J Assoc Physicians India; 2013 Nov; 61(11):832-4. PubMed ID: 24974500
[TBL] [Abstract][Full Text] [Related]
12. Char syndrome, a familial form of patent ductus arteriosus, with a new finding: hypoplasia [corrected] of the 3rd finger.
Babaoğlu K; Oruç M; Günlemez A; Gelb BD
Anadolu Kardiyol Derg; 2012 Sep; 12(6):523-4. PubMed ID: 22728731
[No Abstract] [Full Text] [Related]
13. A 6Mb deletion in band 2q22 due to a complex chromosome rearrangement associated with severe psychomotor retardation, microcephaly and distinctive dysmorphic facial features.
Hoffer MJ; Hilhorst-Hofstee Y; Knijnenburg J; Hansson KB; Engelberts AC; Laan LA; Bakker E; Rosenberg C
Eur J Med Genet; 2007; 50(2):149-54. PubMed ID: 17223398
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [Trisomy 22. A new case].
Berger R; Lejeune C; de Paillerets F
Ann Pediatr (Paris); 1976 Nov; 23(11):705-11. PubMed ID: 16106879
[No Abstract] [Full Text] [Related]
16. [Patent ductus arteriosus in premature infants].
Bratlid D; Farstad T
Tidsskr Nor Laegeforen; 2009 Aug; 129(15):1455-8. PubMed ID: 19690594
[TBL] [Abstract][Full Text] [Related]
17. Lateral facial clefts: a case report.
de Die-Smulders CE; Moog U; Engelen JJ; Peters JJ; Damen A; Vos W; Fryns JP
Genet Couns; 2001; 12(2):163-5. PubMed ID: 11491312
[TBL] [Abstract][Full Text] [Related]
18. Joubert syndrome associated with patent ductus arteriosus in a newborn infant.
Peker E; Kirimi E; Sal E; Ceylan A; Ustyol L; Caksen H
Genet Couns; 2009; 20(3):289-92. PubMed ID: 19852437
[No Abstract] [Full Text] [Related]
19. [Adult mitral and tricuspid valve regurgitation due to patent ductus arteriosus combined with atrial fibrillation; report of a case].
Yoshida K; Tobe S; Adachi K; Kawata M
Kyobu Geka; 2004 Nov; 57(12):1127-30. PubMed ID: 15553030
[TBL] [Abstract][Full Text] [Related]
20. Megalencephaly, polymicrogyria, and hydrocephalus (MPPH) syndrome: a new case with syndactyly.
Pisano T; Meloni M; Cianchetti C; Falchi M; Nucaro A; Pruna D
J Child Neurol; 2008 Aug; 23(8):916-8. PubMed ID: 18474936
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]