127 related articles for article (PubMed ID: 15930908)
21. Brief clinical report: the syndrome of Yunis and Varón--report of a further case.
Hughes HE; Partington MW
Am J Med Genet; 1983 Mar; 14(3):539-44. PubMed ID: 6859104
[No Abstract] [Full Text] [Related]
22. Meier-Gorlin syndrome.
Feingold M
Am J Med Genet; 2002 May; 109(4):338. PubMed ID: 11992493
[No Abstract] [Full Text] [Related]
23. Musculoskeletal manifestations of Russell-Silver syndrome.
Abraham E; Altiok H; Lubicky JP
J Pediatr Orthop; 2004; 24(5):552-64. PubMed ID: 15308907
[TBL] [Abstract][Full Text] [Related]
24. Clinical and genetic heterogeneity of Seckel syndrome.
Faivre L; Le Merrer M; Lyonnet S; Plauchu H; Dagoneau N; Campos-Xavier AB; Attia-Sobol J; Verloes A; Munnich A; Cormier-Daire V
Am J Med Genet; 2002 Nov; 112(4):379-83. PubMed ID: 12376940
[TBL] [Abstract][Full Text] [Related]
25. Microcephaly is not mandatory for the diagnosis of mosaic variegated aneuploidy syndrome.
Callier P; Faivre L; Cusin V; Marle N; Thauvin-Robinet C; Sandre D; Rousseau T; Sagot P; Lacombe E; Faber V; Mugneret F
Am J Med Genet A; 2005 Aug; 137(2):204-7. PubMed ID: 16059936
[TBL] [Abstract][Full Text] [Related]
26. Syndrome of cleft palate, microcephaly, large ears, and short stature (Say syndrome).
Abu-Libdeh B; Fujimoto A; Ehinger M
Am J Med Genet; 1993 Feb; 45(3):358-60. PubMed ID: 8434624
[TBL] [Abstract][Full Text] [Related]
27. Digital anomalies, microcephaly, and normal intelligence: new syndrome or Feingold syndrome?
Kawame H; Pagon RA; Hudgins L
Am J Med Genet; 1997 Mar; 69(3):240-4. PubMed ID: 9096751
[TBL] [Abstract][Full Text] [Related]
28. VATER--tibia aplasia association: report on two patients.
Spruijt L; Devriendt K; Offermans J; Bulstra S; Schrander-Stumpel C
Clin Dysmorphol; 2002 Oct; 11(4):283-7. PubMed ID: 12401995
[TBL] [Abstract][Full Text] [Related]
29. Lujan-Fryns syndrome (X-linked mental retardation with marfanoid habitus): report of three cases and review.
Lacombe D; Bonneau D; Verloes A; Couet D; Koulischer L; Battin J
Genet Couns; 1993; 4(3):193-8. PubMed ID: 8267926
[TBL] [Abstract][Full Text] [Related]
30. Growth deficiency, facial anomalies, and brachydactyly (Frías syndrome): a second family.
Martínez-Frías ML; Toral JF; López-Grondona F; Mendioroz J; Bermejo E
Am J Med Genet A; 2005 Sep; 137A(3):288-91. PubMed ID: 16088912
[TBL] [Abstract][Full Text] [Related]
31. Esophageal atresia, hypoplasia of zygomatic complex, microcephaly, cup-shaped ears, congenital heart defect, and mental retardation--new MCA/MR syndrome in two affected sibs and a mildly affected mother?
Wieczorek D; Shaw-Smith C; Kohlhase J; Schmitt W; Buiting K; Coffey A; Howard E; Hehr U; Gillessen-Kaesbach G
Am J Med Genet A; 2007 Jun; 143A(11):1135-42. PubMed ID: 17497718
[TBL] [Abstract][Full Text] [Related]
32. Brachydactylic multiple delta phalanges plus syndrome.
Ahn CP; Lachman RS; Cox VA; Blumberg B; Klein OD
Am J Med Genet A; 2005 Sep; 138(1):41-4. PubMed ID: 16092122
[TBL] [Abstract][Full Text] [Related]
33. Myhre syndrome: new reports, review, and differential diagnosis.
Burglen L; Héron D; Moerman A; Dieux-Coeslier A; Bourguignon JP; Bachy A; Carel JC; Cormier-Daire V; Manouvrier S; Verloes A
J Med Genet; 2003 Jul; 40(7):546-51. PubMed ID: 12843331
[No Abstract] [Full Text] [Related]
34. Feingold syndome: a rare but important cause of syndromic tracheoesophageal fistula.
Layman-Pleet L; Jackson CC; Chou S; Boycott KM
J Pediatr Surg; 2007 Sep; 42(9):E1-3. PubMed ID: 17848225
[TBL] [Abstract][Full Text] [Related]
35. Angel shaped phalangeal dysplasia, hip dysplasia, and positional teeth abnormalities are part of the brachydactyly C spectrum associated with CDMP-1 mutations.
Holder-Espinasse M; Escande F; Mayrargue E; Dieux-Coeslier A; Fron D; Doual-Bisser A; Boute-Benejean O; Robert Y; Porchet N; Manouvrier-Hanu S
J Med Genet; 2004 Jun; 41(6):e78. PubMed ID: 15173244
[No Abstract] [Full Text] [Related]
36. Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype.
Tedesco MG; Lonardo F; Ceccarini C; Cesarano C; Digilio MC; Magliozzi M; Rogaia D; Mencarelli A; Leoni C; Piscopo C; Imperatore V; Falco MT; Fontana P; Nardone AM; Novelli A; Troiani S; Seri M; Prontera P
Am J Med Genet A; 2021 Apr; 185(4):1204-1210. PubMed ID: 33442900
[TBL] [Abstract][Full Text] [Related]
37. Dominant inheritance of microcephaly, short stature and congenital dislocation of the hips.
Newbury-Ecob RA; Young ID
Clin Dysmorphol; 1993 Jan; 2(1):34-8. PubMed ID: 8298736
[TBL] [Abstract][Full Text] [Related]
38. Myhre's syndrome in a girl with normal intelligence.
Rulli I; Ferrero GB; Belligni E; Delmonaco AG; Defilippi C; Silengo M
Am J Med Genet A; 2005 Apr; 134A(1):100-2. PubMed ID: 15723310
[No Abstract] [Full Text] [Related]
39. A new syndrome with cardiac malformation, cleft lip-palate, microcephaly and digital anomalies?
Perçin EF; Düzcan F; Kafali G; Sezgin I
Clin Genet; 1995 Nov; 48(5):264-7. PubMed ID: 8825606
[TBL] [Abstract][Full Text] [Related]
40. Microdeletions of chromosome 7p21, including TWIST1, associated with significant microcephaly, facial dysmorphism, and short stature.
Busche A; Graul-Neumann LM; Zweier C; Rauch A; Klopocki E; Horn D
Eur J Med Genet; 2011; 54(3):256-61. PubMed ID: 21333765
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]