99 related articles for article (PubMed ID: 6100620)
1. Recent advances in cytogenetics.
Gorlin RJ
Mead Johnson Symp Perinat Dev Med; 1983; (22):12-22. PubMed ID: 6100620
[No Abstract] [Full Text] [Related]
2. [Chromosomal pathology. Recent advances].
Giraud F; Mattei JF
Arch Fr Pediatr; 1985 Mar; 42(3):159-62. PubMed ID: 2988476
[No Abstract] [Full Text] [Related]
3. Contiguous gene syndromes: a component of recognizable syndromes.
Schmickel RD
J Pediatr; 1986 Aug; 109(2):231-41. PubMed ID: 3016222
[No Abstract] [Full Text] [Related]
4. High-resolution cytogenetics.
Yunis JJ; Lewandowski RC
Birth Defects Orig Artic Ser; 1983; 19(5):11-37. PubMed ID: 6309269
[No Abstract] [Full Text] [Related]
5. [Newly discovered structural chromosome aberrations in long familial syndromes, associations and sequences. Prader-Willi syndrome, Miller-Dieker syndrome, Giedion-Langer syndrome, Aniridia-Wilms' tumor association, DiGeorge sequence, Wiedemann-Beckwith syndrome].
Schinzel A
Ergeb Inn Med Kinderheilkd; 1988; 57():57-75. PubMed ID: 2850909
[No Abstract] [Full Text] [Related]
6. [Chromosome microdeletions].
de Grouchy J
Arch Fr Pediatr; 1983 Jan; 40(1):1-3. PubMed ID: 6305301
[No Abstract] [Full Text] [Related]
7. Toward clinical microcytogenetics: the aniridia and the retinoblastoma stories.
de Grouchy J
Prog Clin Biol Res; 1982; 103 Pt B():359-67. PubMed ID: 6298811
[TBL] [Abstract][Full Text] [Related]
8. Microcytogenetics 1984.
de Grouchy J; Turleau C
Experientia; 1986 Oct; 42(10):1090-7. PubMed ID: 3533601
[No Abstract] [Full Text] [Related]
9. [Molecular advances in "non-mendelian" genetics. Implications for pediatrics].
Pérez Jurado LA
An Esp Pediatr; 1993 Jun; 38(6):479-87. PubMed ID: 8368674
[No Abstract] [Full Text] [Related]
10. Deletion of chromosome 15 (q11-13) in a Prader-Labhart-Willi syndrome clinic population.
Cassidy SB; Thuline HC; Holm VA
Am J Med Genet; 1984 Feb; 17(2):485-95. PubMed ID: 6336316
[TBL] [Abstract][Full Text] [Related]
11. Cytogenetic diagnosis of genetic diseases.
Shapiro LR; Wilmot PL
Pediatr Ann; 1993 May; 22(5):298-303. PubMed ID: 8510996
[No Abstract] [Full Text] [Related]
12. The significance of genetic research in ophthalmology.
Francois J
Birth Defects Orig Artic Ser; 1982; 18(6):3-25. PubMed ID: 6293603
[No Abstract] [Full Text] [Related]
13. [New knowledge and methods of cytogenetics].
Körner H
Z Arztl Fortbild (Jena); 1988; 82(22):1153-7. PubMed ID: 3073594
[No Abstract] [Full Text] [Related]
14. [Cytogenetics of juvenile tumors].
Fonatsch C
Dtsch Med Wochenschr; 1985 Aug; 110(33):1257-65. PubMed ID: 2990845
[No Abstract] [Full Text] [Related]
15. Use of FISH technique in the diagnosis of chromosomal syndromes.
Iqbal MA; Ulmer C; Sakati N
East Mediterr Health J; 1999 Nov; 5(6):1218-24. PubMed ID: 11924115
[TBL] [Abstract][Full Text] [Related]
16. Genomic imprinting relevant to genetic diseases.
Niikawa N
Southeast Asian J Trop Med Public Health; 1997; 28 Suppl 3():46-57. PubMed ID: 9640600
[TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of chromosome 15 abnormalities in the Prader-Willi/Angelman syndrome region by traditional and molecular cytogenetics.
Toth-Fejel S; Magenis RE; Leff S; Brown MG; Comegys B; Lawce H; Berry T; Kesner D; Webb MJ; Olson S
Am J Med Genet; 1995 Feb; 55(4):444-52. PubMed ID: 7762584
[TBL] [Abstract][Full Text] [Related]
18. Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: an overview.
Knoll JH; Wagstaff J; Lalande M
Am J Med Genet; 1993 Apr; 46(1):2-6. PubMed ID: 8388170
[TBL] [Abstract][Full Text] [Related]
19. Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader-Willi syndrome and Angelman syndrome.
Delach JA; Rosengren SS; Kaplan L; Greenstein RM; Cassidy SB; Benn PA
Am J Med Genet; 1994 Aug; 52(1):85-91. PubMed ID: 7977469
[TBL] [Abstract][Full Text] [Related]
20. Social phenotypes in neurogenetic syndromes.
Feinstein C; Singh S
Child Adolesc Psychiatr Clin N Am; 2007 Jul; 16(3):631-47. PubMed ID: 17562583
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]