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A Baumer

Showing results (51-60 of 63) with videos related to

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Psychiatry Research|June 16, 1997
Variants in neurotrophic factor genes and schizophrenic psychoses: no associations in a Spanish populationJ Thome, N Durany, A Palomo, et al.
Annals of the New York Academy of Sciences|December 26, 1992
Mitochondrial DNA mutation associated with aging and degenerative diseaseP Nagley, I R Mackay, A Baumer, et al.
Physical Review Letters|November 5, 2004
Strong temperature dependence of irradiation effects in organic layersP Feulner, T Niedermayer, K Eberle, et al.
American Journal of Human Genetics|March 31, 2000
A novel locus (DFNA24) for prelingual nonprogressive autosomal dominant nonsyndromic hearing loss maps to 4q35-qter in a large Swiss German kindredF M Häfner, A A Salam, T E Linder, et al.
Human Genetics|January 7, 1998
Clinical and genetic heterogeneity in Meckel syndromeP Paavola, R Salonen, A Baumer, et al.
Annals of Human Genetics|October 19, 2006
Jacobsen syndrome and Beckwith-Wiedemann syndrome caused by a parental pericentric inversion inv(11)(p15q24)D Gadzicki, A Baumer, E Wey, et al.
Journal of Medical Genetics|December 11, 2008
Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypesD Bartholdi, M Krajewska-Walasek, K Ounap, et al.
Neuroreport|May 31, 1996
A null mutation allele in the CNTF gene and schizophrenic psychosesJ Thome, N Durany, A Harsányi, et al.
European Journal of Pediatrics|May 2, 2000
Maternal uniparental disomy 7--review and further delineation of the phenotypeD Kotzot, D Balmer, A Baumer, et al.
Journal of Medical Genetics|November 17, 2007
Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formationE Rossi, M Riegel, J Messa, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
Psychiatry Research|June 16, 1997
Variants in neurotrophic factor genes and schizophrenic psychoses: no associations in a Spanish populationJ Thome, N Durany, A Palomo, et al.
Annals of the New York Academy of Sciences|December 26, 1992
Mitochondrial DNA mutation associated with aging and degenerative diseaseP Nagley, I R Mackay, A Baumer, et al.
Physical Review Letters|November 5, 2004
Strong temperature dependence of irradiation effects in organic layersP Feulner, T Niedermayer, K Eberle, et al.
American Journal of Human Genetics|March 31, 2000
A novel locus (DFNA24) for prelingual nonprogressive autosomal dominant nonsyndromic hearing loss maps to 4q35-qter in a large Swiss German kindredF M Häfner, A A Salam, T E Linder, et al.
Human Genetics|January 7, 1998
Clinical and genetic heterogeneity in Meckel syndromeP Paavola, R Salonen, A Baumer, et al.
Annals of Human Genetics|October 19, 2006
Jacobsen syndrome and Beckwith-Wiedemann syndrome caused by a parental pericentric inversion inv(11)(p15q24)D Gadzicki, A Baumer, E Wey, et al.
Journal of Medical Genetics|December 11, 2008
Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypesD Bartholdi, M Krajewska-Walasek, K Ounap, et al.
Neuroreport|May 31, 1996
A null mutation allele in the CNTF gene and schizophrenic psychosesJ Thome, N Durany, A Harsányi, et al.
European Journal of Pediatrics|May 2, 2000
Maternal uniparental disomy 7--review and further delineation of the phenotypeD Kotzot, D Balmer, A Baumer, et al.
Journal of Medical Genetics|November 17, 2007
Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formationE Rossi, M Riegel, J Messa, et al.
Pageof 7