92 related articles for article (PubMed ID: 15608400)
41. Assessment of DPY19L2 Deletion in Familial and Non-Familial Individuals with Globozoospermia and DPY19L2 Genotyping.
Modarres P; Tanhaei S; Tavalaee M; Ghaedi K; Deemeh MR; Nasr-Esfahani MH
Int J Fertil Steril; 2016; 10(2):196-207. PubMed ID: 27441053
[TBL] [Abstract][Full Text] [Related]
42. Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan Africa.
Sangaré M; Hendrickson B; Sango HA; Chen K; Nofziger J; Amara A; Dutra A; Schindler AB; Guindo A; Traoré M; Harmison G; Pak E; Yaro FN; Bricceno K; Grunseich C; Chen G; Boehm M; Zukosky K; Bocoum N; Meilleur KG; Daou F; Bagayogo K; Coulibaly YI; Diakité M; Fay MP; Lee HS; Saad A; Gribaa M; Singleton AB; Maiga Y; Auh S; Landouré G; Fairhurst RM; Burnett BG; Scholl T; Fischbeck KH
Ann Neurol; 2014 Apr; 75(4):525-32. PubMed ID: 24515897
[TBL] [Abstract][Full Text] [Related]
43. Determination of exon 7 SMN1 deletion in Iranian patients and heterozygous carriers by quantitative real-time PCR.
Akbari MT; Noruzinia M; Mozdarani H; Hamid M
J Genet; 2011 Apr; 90(1):133-6. PubMed ID: 21677399
[No Abstract] [Full Text] [Related]
44. Carrier screening for spinal muscular atrophy (SMA) in 107,611 pregnant women during the period 2005-2009: a prospective population-based cohort study.
Su YN; Hung CC; Lin SY; Chen FY; Chern JP; Tsai C; Chang TS; Yang CC; Li H; Ho HN; Lee CN
PLoS One; 2011 Feb; 6(2):e17067. PubMed ID: 21364876
[TBL] [Abstract][Full Text] [Related]
45. Marked geographic aggregation of acute intermittent porphyria families carrying mutation Q180X in Venezuelan populations, with description of further mutations.
Paradisi I; Arias S
J Inherit Metab Dis; 2010 Dec; 33 Suppl 3():S455-63. PubMed ID: 20978940
[TBL] [Abstract][Full Text] [Related]
46. Molecular characterization of SMN copy number derived from carrier screening and from core families with SMA in a Chinese population.
Sheng-Yuan Z; Xiong F; Chen YJ; Yan TZ; Zeng J; Li L; Zhang YN; Chen WQ; Bao XH; Zhang C; Xu XM
Eur J Hum Genet; 2010 Sep; 18(9):978-84. PubMed ID: 20442745
[TBL] [Abstract][Full Text] [Related]
47. Robust quantification of the SMN gene copy number by real-time TaqMan PCR.
Gómez-Curet I; Robinson KG; Funanage VL; Crawford TO; Scavina M; Wang W
Neurogenetics; 2007 Nov; 8(4):271-8. PubMed ID: 17647030
[TBL] [Abstract][Full Text] [Related]
48. An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA).
Wirth B
Hum Mutat; 2000; 15(3):228-37. PubMed ID: 10679938
[TBL] [Abstract][Full Text] [Related]
49. Quantitative analysis of SMN1 gene and estimation of SMN1 deletion carrier frequency in Korean population based on real-time PCR.
Lee TM; Kim SW; Lee KS; Jin HS; Koo SK; Jo I; Kang S; Jung SC
J Korean Med Sci; 2004 Dec; 19(6):870-3. PubMed ID: 15608400
[TBL] [Abstract][Full Text] [Related]
50. Population screening and cascade testing for carriers of SMA.
Smith M; Calabro V; Chong B; Gardiner N; Cowie S; du Sart D
Eur J Hum Genet; 2007 Jul; 15(7):759-66. PubMed ID: 17392705
[TBL] [Abstract][Full Text] [Related]
51. Detection of spinal muscular atrophy carriers by nested polymerase chain reaction of single sperm cells.
Yaron Y; Cohen T; Mey-Raz N; Schwartz T; Amit A; Malcov M
Genet Test; 2006; 10(1):18-23. PubMed ID: 16544998
[TBL] [Abstract][Full Text] [Related]
52. Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: a highly efficient and reliable carrier-screening test.
Su YN; Hung CC; Li H; Lee CN; Cheng WF; Tsao PN; Chang MC; Yu CL; Hsieh WS; Lin WL; Hsu SM
Hum Mutat; 2005 May; 25(5):460-7. PubMed ID: 15832310
[TBL] [Abstract][Full Text] [Related]
53. Genetic testing and risk assessment for spinal muscular atrophy (SMA).
Ogino S; Wilson RB
Hum Genet; 2002 Dec; 111(6):477-500. PubMed ID: 12436240
[TBL] [Abstract][Full Text] [Related]
54. Carrier frequency of SMA by quantitative analysis of the SMN1 deletion in the Iranian population.
Hasanzad M; Azad M; Kahrizi K; Saffar BS; Nafisi S; Keyhanidoust Z; Azimian M; Refah AA; Also E; Urtizberea JA; Tizzano EF; Najmabadi H
Eur J Neurol; 2010 Jan; 17(1):160-2. PubMed ID: 19538222
[TBL] [Abstract][Full Text] [Related]
55. Determination of SMN1 and SMN2 copy number using TaqMan technology.
Anhuf D; Eggermann T; Rudnik-Schöneborn S; Zerres K
Hum Mutat; 2003 Jul; 22(1):74-8. PubMed ID: 12815596
[TBL] [Abstract][Full Text] [Related]
56.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
57.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
58.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
59.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
60.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]