353 related articles for article (PubMed ID: 8031534)
41. Neuroblastoma in patients with constitutional chromosomal changes.
Fryns JP
Genet Couns; 1996; 7(1):73. PubMed ID: 8652093
[No Abstract] [Full Text] [Related]
42. The 8p-syndrome.
Ostergaard GZ; Tommerup N
Ann Genet; 1989; 32(2):87-91. PubMed ID: 2667457
[TBL] [Abstract][Full Text] [Related]
43. Interstitial deletion of the long arm of chromosome 11.
Carnevale A; Blanco B; Grether P; Castillejos AR
Ann Genet; 1987; 30(1):56-8. PubMed ID: 3498432
[TBL] [Abstract][Full Text] [Related]
44. De novo deletion of chromosome 9 (9p-) in a child with multiple congenital anomalies and psychomotor retardation.
Murthy DS; Murthy SK; Banker GJ; Patel AJ
Indian Pediatr; 1991 May; 28(5):546-9. PubMed ID: 1684352
[No Abstract] [Full Text] [Related]
45. A familial paracentric inv(1)(q42q44) resulting in a child with a del(1)(q42) karyotype.
Speevak M; Hunter AG; Hughes H; Cox DM
Ann Genet; 1985; 28(3):177-80. PubMed ID: 3879153
[TBL] [Abstract][Full Text] [Related]
46. Fryns syndrome: another example of non-lethal outcome with severe mental handicap.
Hanssen AM; Schrander-Stumpel CT; Thiry PA; Fryns JP
Genet Couns; 1992; 3(4):187-93. PubMed ID: 1472353
[TBL] [Abstract][Full Text] [Related]
47. Familial hiatus hernia and gastro-oesophageal reflux.
Chana J; Crabbe DC; Spitz L
Eur J Pediatr Surg; 1996 Jun; 6(3):175-6. PubMed ID: 8817214
[TBL] [Abstract][Full Text] [Related]
48. [Killian-Teschler-Nicola syndrome (Pallister-Killian syndrome, mosaic tetrasomy 12p)].
Pankau R; Diebold U; Jenderny J; Kautza M; Dörner K
Monatsschr Kinderheilkd; 1992 Jun; 140(6):340-2. PubMed ID: 1640944
[No Abstract] [Full Text] [Related]
49. [A patient with ring chromosome 13].
Hammond A; Bijlsma JB
Ned Tijdschr Geneeskd; 1981 May; 125(19):752-5. PubMed ID: 7242723
[No Abstract] [Full Text] [Related]
50. Interstitial deletion of 10q: clinical features and literature review.
Lobo S; Cervenka J; London A; Pierpont ME
Am J Med Genet; 1992 Jul; 43(4):701-3. PubMed ID: 1621761
[TBL] [Abstract][Full Text] [Related]
51. Costello syndrome: a postnatal growth retardation syndrome with distinct phenotype.
Fryns JP; Vogels A; Haegeman J; Eggermont E; van den Berghe H
Genet Couns; 1994; 5(4):337-43. PubMed ID: 7888135
[TBL] [Abstract][Full Text] [Related]
52. Tau syndrome (thrombocytopenia and absent ulnar) with mental retardation and facial dysmorphy.
Stoll C; Finck S; Janser B; Printz M; Lutz P
Genet Couns; 1992; 3(1):41-7. PubMed ID: 1590980
[TBL] [Abstract][Full Text] [Related]
53. Chromosome 11 long arm partial deletion: a new syndrome.
Engel E; Hirshberg CS; Cassidy SB; McGee BJ
Am J Ment Defic; 1976 Jan; 80(4):473-5. PubMed ID: 1247044
[TBL] [Abstract][Full Text] [Related]
54. Choanal atresia in a patient with the deletion (9p) syndrome.
Shashi V; Golden WL; Fryburg JS
Am J Med Genet; 1994 Jan; 49(1):88-90. PubMed ID: 8172257
[TBL] [Abstract][Full Text] [Related]
55. ["De novo" partial trisomy 16p (author's transl)].
Gabarrón Llamas J; Cabrerizo Portero D; Montserrat Bernal F; Rodríguez Costa T; Cabrerizo Merino C; Rodríguez López F
An Esp Pediatr; 1981 Dec; 15(6):587-91. PubMed ID: 7337311
[TBL] [Abstract][Full Text] [Related]
56. A case of ring (9)/del(9p) mosaicism associated with gastroesophageal reflux.
Leung AK; Rudd NL
Am J Med Genet; 1988 Jan; 29(1):43-8. PubMed ID: 3344775
[TBL] [Abstract][Full Text] [Related]
57. Pallister-Killian Syndrome (PKS) as a Cause of Mental Retardation.
Shamdeen A; Meyer S; Gottschling S; Oehl-Jaschkowitz B; Gortner L; Shamdeen MG
Klin Padiatr; 2009; 221(2):97-9. PubMed ID: 19067289
[TBL] [Abstract][Full Text] [Related]
58. A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?
van Buggenhout G; Decock P; Fryns JP
Genet Couns; 1996; 7(1):53-9. PubMed ID: 8652089
[TBL] [Abstract][Full Text] [Related]
59. [Ring chromosome 14. I. A case report on homogeneous r(14)].
Raoul O; Razavi F; Lescs MC; Bouhanna A
Ann Genet; 1984; 27(2):88-90. PubMed ID: 6331795
[TBL] [Abstract][Full Text] [Related]
60. Clinical outcomes of four patients with microdeletion in the long arm of chromosome 2.
McMilin KD; Reiss JA; Brown MG; Black MH; Buckmaster DA; Durum CT; Gunter KA; Lawce HJ; Berry TL; Lamb OA; Olson CL; Weeks FF; Yoshitomi MJ; Jacky PB; Olson SB; Magenis RE
Am J Med Genet; 1998 Jun; 78(1):36-43. PubMed ID: 9637421
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
