GENETIC COUNSELING[ta] - Search Results

Year	Number of Results
1990	38
1991	39
1992	40
1993	53
1994	56
1995	42
1996	48
1997	47
1998	50
1999	55
2000	48
2001	50
2002	59
2003	61
2004	65
2005	61
2006	62
2007	54
2008	53
2009	47
2010	58
2011	56
2012	68
2013	65
2014	64
2015	69
2016	67
2024	0

1

Witters I, Bogaerts A, Fryns JP. Witters I, et al. Genet Couns. 2010;21(2):169-82. Genet Couns. 2010. PMID: 20681217

2

Genetic counseling in Usher syndrome: linkage and mutational analysis of 10 Colombian families.

Tamayo ML, Lopez G, Gelvez N, Medina D, Kimberling WJ, Rodríguez V, Tamayo GE, Bernal JE. Tamayo ML, et al. Genet Couns. 2008;19(1):15-27. Genet Couns. 2008. PMID: 18564497

3

Hanhart syndrome.

Dogan DG, Dogan M, Aslan M, Menekse E, Yakinci C. Dogan DG, et al. Genet Couns. 2010;21(4):359-62. Genet Couns. 2010. PMID: 21290964

4

A case with bilateral radio-ulnar synostosis.

Koç A, Kaymak AO, Karaer K, Ergün MA, Aksu T, Perçin EF. Koç A, et al. Genet Couns. 2008;19(2):193-8. Genet Couns. 2008. PMID: 18618994 Review.

5

Duchenne muscular dystrophy in a developing country: challenges in management and genetic counseling.

López-Hernández LB, Gómez-Díaz B, Escobar-Cedillo RE, Gama-Moreno O, Camacho-Molina A, Soto-Valdés DM, Anaya-Segura MA, Luna-Padrón E, Zúñiga-Guzmán C, Lopez-Hernández JA, Vázquez-Cárdenas NA, Sánchez-Chapul L, Rangel-Villalobos H, Canto P, López-Cardona MG, García S, Méndez-Covarrubias G, Coral-Vázquez RM. López-Hernández LB, et al. Genet Couns. 2014;25(2):129-41. Genet Couns. 2014. PMID: 25059011

6

Mixed gonadal dysgenesis with 45,X/46,X,idic(Y)/46,XY,idic(Y) karyotype.

Caglayan AO, Demiryilmaz F, Kendirci M, Ozyazgan I, Akalin H, Bittmann S. Caglayan AO, et al. Genet Couns. 2009;20(2):173-9. Genet Couns. 2009. PMID: 19650415

7

Ectrodactyly and tetralogy of Fallot in a fetus with del(6)(q21q23).

Novikova IV, Lazarevich AA, Egorova TM, Solovyeva IV, Golovataja EI, Plevako TA, Mikheeva NG, Lurie IW. Novikova IV, et al. Genet Couns. 2014;25(1):19-27. Genet Couns. 2014. PMID: 24783651 Review.

8

MECP2 DUPLICATION SYNDROME WITH ADDITIONAL FINDINGS.

Tug E, Ergun MA, Percin EF. Tug E, et al. Genet Couns. 2016;27(4):471-478. Genet Couns. 2016. PMID: 30226965

9

Deafness on the island of Providencia - Colombia: different etiology, different genetic counseling.

Lattig MC, Gelvez N, Plaza SL, Tamayo G, Uribe JI, Salvatierra I, Bernal JE, Tamayo ML. Lattig MC, et al. Genet Couns. 2008;19(4):403-12. Genet Couns. 2008. PMID: 19239084

10

Congenital mirror hand deformity.

Arayici S, Simsek GK, Oncel MY, Erdeve O, Dilmen U. Arayici S, et al. Genet Couns. 2012;23(3):393-6. Genet Couns. 2012. PMID: 23072188

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