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Formal genetics of Fanconi's anemia.
Schroeder TM, Tilgen D, Krüger J, Vogel F. Schroeder TM, et al. Hum Genet. 1976 Jun 29;32(3):257-88. doi: 10.1007/BF00295817. Hum Genet. 1976. PMID: 939547
A genetic and anthropological study of atlanto-occipital fusion.
Kalla AK, Khanna S, Singh IP, Sharma S, Schnobel R, Vogel F. Kalla AK, et al. Hum Genet. 1989 Jan;81(2):105-12. doi: 10.1007/BF00293884. Hum Genet. 1989. PMID: 2912881 Clinical Trial.
The development of human genetics in Germany; a personal view.
Vogel F. Vogel F. Hum Genet. 2005 Jul;117(2-3):278-84. doi: 10.1007/s00439-005-1312-1. Hum Genet. 2005. PMID: 15886996
Recurrent mutation pressure does not explain the prevalence of the marker (X) syndrome.
Vogel F, Krüger J, Nielsen KB, Fryns JP, Schindler D, Schinzel A, Schmidt A, Schwinger E. Vogel F, et al. Hum Genet. 1985;71(1):1-6. doi: 10.1007/BF00295657. Hum Genet. 1985. PMID: 3861564
Mutation and selection in the marker (X) syndrome. A hypothesis.
Vogel F. Vogel F. Ann Hum Genet. 1984 Oct;48(4):327-32. doi: 10.1111/j.1469-1809.1984.tb00846.x. Ann Hum Genet. 1984. PMID: 6497350
Spontaneous mutation in man.
Vogel F, Rathenberg R. Vogel F, et al. Adv Hum Genet. 1975;5:223-318. doi: 10.1007/978-1-4615-9068-2_4. Adv Hum Genet. 1975. PMID: 805513 Review. No abstract available.
HLA antigen, gene, and haplotype frequencies in Thailand.
Greiner J, Schleiermacher E, Lenhard V, Kulapongs P, Vogel F. Greiner J, et al. Hum Genet. 1978 Feb 23;41(1):73-87. doi: 10.1007/BF00278873. Hum Genet. 1978. PMID: 631862
A genetic study of the human low-voltage electroencephalogram.
Anokhin A, Steinlein O, Fischer C, Mao Y, Vogt P, Schalt E, Vogel F. Anokhin A, et al. Hum Genet. 1992 Sep-Oct;90(1-2):99-112. doi: 10.1007/BF00210751. Hum Genet. 1992. PMID: 1427795
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