103 related articles for article (PubMed ID: 8357010)
21. Craniosynostosis and marfanoid habitus without mental retardation: report of a third case.
Mégarbané A; Hokayem N
Am J Med Genet; 1998 May; 77(2):170-1. PubMed ID: 9605294
[No Abstract] [Full Text] [Related]
22. Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.
Leonardi ML; Pai GS; Wilkes B; Lebel RR
Am J Med Genet; 2001 Aug; 102(3):237-42. PubMed ID: 11484200
[TBL] [Abstract][Full Text] [Related]
23. Fetus with features of Crane-Heise syndrome and aminopterin syndrome sine aminopterin (ASSAS).
Barnicoat AJ; Seller MJ; Bennett CP
Clin Dysmorphol; 1994 Oct; 3(4):353-7. PubMed ID: 7894742
[TBL] [Abstract][Full Text] [Related]
24. Megalocornea-mental retardation syndrome: an additional case report.
Naritomi K; Chinen Y; Tohma T
Jpn J Hum Genet; 1997 Sep; 42(3):461-5. PubMed ID: 12503196
[TBL] [Abstract][Full Text] [Related]
25. Osteosarcoma in a 16-year-old boy with Baller-Gerold syndrome.
Preis S; Majewski F; Körholz D; Göbel U
Clin Dysmorphol; 1995 Apr; 4(2):161-8. PubMed ID: 7606324
[TBL] [Abstract][Full Text] [Related]
26. Opitz (BBB/G) syndrome: oral manifestations.
Brooks JK; Leonard CO; Coccaro PJ
Am J Med Genet; 1992 Jun; 43(3):595-601. PubMed ID: 1605255
[TBL] [Abstract][Full Text] [Related]
27. [Ring chromosome 8: microcephaly, mental retardation and minor facial anomalies with adhesive behavioral phenotype].
Bibas Bonet H; Fontenla M; Fauze R; G de Pinat I
Rev Neurol; 2001 Apr 16-30; 32(8):746-50. PubMed ID: 11391511
[TBL] [Abstract][Full Text] [Related]
28. Possible third case of Lin-Gettig syndrome.
Hedera P; Innis JW
Am J Med Genet; 2002 Jul; 110(4):380-3. PubMed ID: 12116213
[TBL] [Abstract][Full Text] [Related]
29. Clinical and behavioral characteristics in FG syndrome.
Graham JM; Superneau D; Rogers RC; Corning K; Schwartz CE; Dykens EM
Am J Med Genet; 1999 Aug; 85(5):470-5. PubMed ID: 10405444
[TBL] [Abstract][Full Text] [Related]
30. Juberg-Marsidi syndrome: report of an additional case.
Tsukahara M; Nasu T; Takihara H; Hattori Y; Nakane H; Kamata K; Mitsui H; Hayashida S
Am J Med Genet; 1995 Sep; 58(4):353-5. PubMed ID: 8533845
[TBL] [Abstract][Full Text] [Related]
31. [Soto's syndrome (cerebral gigantism)].
Jović NS; Vranjesević DN; Jović JZ; Marinković DD
Srp Arh Celok Lek; 1996; 124(1-2):37-40. PubMed ID: 9102812
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Kabuki make-up syndrome with unilateral renal agenesis.
Rosti RO; Kayserili H
Turk J Pediatr; 2009; 51(3):298-300. PubMed ID: 19817278
[TBL] [Abstract][Full Text] [Related]
34. An exceptional Albanian family with seven children presenting with dysmorphic features and mental retardation: maternal phenylketonuria.
Knerr I; Zschocke J; Schellmoser S; Topf HG; Weigel C; Dötsch J; Rascher W
BMC Pediatr; 2005 Apr; 5(1):5. PubMed ID: 15811181
[TBL] [Abstract][Full Text] [Related]
35. Syndrome of arachnodactyly, disturbance of cranial ossification, protruding eyes, feeding difficulties, and mental retardation.
Kosztolányi G; Weisenbach J; Méhes K
Am J Med Genet; 1995 Sep; 58(3):213-6. PubMed ID: 8533819
[TBL] [Abstract][Full Text] [Related]
36. Filippi syndrome: report of three additional cases.
Williams MS; Williams JL; Wargowski DS; Pauli RM; Pletcher BA
Am J Med Genet; 1999 Nov; 87(2):128-33. PubMed ID: 10533026
[TBL] [Abstract][Full Text] [Related]
37. Sutural exostoses, rib hyperostoses, craniosynostosis, mental retardation with focal fat deposition: Proteus syndrome?
Christianson AL; Van Allen MI
Am J Med Genet; 1996 Dec; 66(2):150-3. PubMed ID: 8958321
[TBL] [Abstract][Full Text] [Related]
38. Chromosome 10p11.2-p12.2 duplication: report of a patient and review of the literature.
Mégarbané A; Gosset P; Souraty N; Lapierre JM; Korban R; Zahed L; Samaras L; Vekemans M; Prieur M
Am J Med Genet; 2001 Dec; 104(3):204-8. PubMed ID: 11754045
[TBL] [Abstract][Full Text] [Related]
39. Craniosynostosis, telecanthus, scalp hair abnormalities, and sensorineural deafness in two sibs.
Mégarbané A; Hersh JH; Chouery E; Fabre M
Am J Med Genet; 2002 May; 109(4):323-7. PubMed ID: 11992488
[TBL] [Abstract][Full Text] [Related]
40. New X-linked mental retardation syndrome with the gene mapped tentatively in Xp22.3.
Wittwer B; Kircheisen R; Leutelt J; Orth U; Gal A
Am J Med Genet; 1996 Jul; 64(1):42-9. PubMed ID: 8826447
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
