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Erika Bühler
Observed names:
E Bühler,
E M Buhler,
E M Bühler,
E. Bühler,
E. M. BUHLER,
E. M. Buhler,
E. M. BÜHLER,
E. M. Bühler,
E.M. Buhler,
E.M. Bühler
show all 10
Institution:
University of Basel
Observed institutions:
University of Geneva,
University of British Columbia,
University of Basel,
University of Pavia,
University of Würzburg,
University Hospital of Basel,
University Children’s Hospital Basel
show all 7
OpenAlex ID:
A5111742532
Congenital Asymmetry Associated With Diploid-triploid Mosaicism and Large Satellites
1964
·
P. Ferrier
, G. Stalder
, et al.
·
The Lancet
·
112
A final word on the tricho‐rhino‐phalangeal syndromes
1987
·
E. M. Bühler
, U. K. Bühler
, et al.
·
Clinical Genetics
·
78
45,X/46,XYq dic-Geschlechtschromosomenmosaik
1975
·
R. O. Frey
, E. M. Bühler
, et al.
·
Human Genetics
·
57
Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndrome.
1992
·
R Tupler
, L Bortotto
, et al.
·
Journal of Medical Genetics
·
45
PDF
Correlation between the number of sex chromosomes and the H-Y antigen titer
1982
·
M. Fraccaro
, Antonia Mayerová
, et al.
·
Human Genetics
·
45
15/15 translocation in Prader-Willi syndrome.
1977
·
M Fraccaro
, O Zuffardi
, et al.
·
Journal of Medical Genetics
·
44
PDF
Chromosomal Translocation in a Mentally Deficient Child with Cryptorchidism
1963
·
E. M. BÜHLER
, R. ROSSIER
, et al.
·
Acta Paediatrica
·
34
Partial Monosomy 18 and Anomaly of Thyroxine Synthesis
1964
·
E.M. Bühler
, U.K. Bühler
, et al.
·
The Lancet
·
33
A family with balanced D1?Cs-translocation carriers and unbalanced offspring
1964
·
G. R. Stalder
, E. M. Buhler
, et al.
·
Human Genetics
·
31
Possible Trisomy in Chromosome Group 6-12
1963
·
G.R. Stalder
, E.M. Buhler
, et al.
·
The Lancet
·
29
Trisomy-18 syndrome caused by translocation or isochromosome formation. A case report with bibliography.
1972
·
H Müller
, E M Bühler
, et al.
·
Journal of Medical Genetics
·
27
PDF
Irregular phenotypic expression of ring chromosomes
1975
·
Rosina Zdansky
, Milly Andrle
, et al.
·
Human Genetics
·
25
Chromosome 15 and Prader‐Willi Syndrome
1978
·
O. Zuffardi
, E. M. Bühler
, et al.
·
Clinical Genetics
·
23
Siblings with Different Types of Chromosal Aberrations Due to D/E-Translocation of the Mother
1966
·
Elisabeth Hauschteck
, Gertrud Mürset
, et al.
·
Cytogenetic and Genome Research
·
23
Presumptive evidence of two active X chromosomes in somatic cells of a human female
1977
·
E. M. BUHLER
, L. P. JURIK
, et al.
·
Nature
·
20
Arrangement of DYZ1 and DYZ2 repeats on the human Y-chromosome: a case with presence of DYZ1 and absence of DYZ2
1992
·
E. Manz
, M. Alkan
, et al.
·
Molecular and Cellular Probes
·
16
Lung hypoplasia and severe pulmonary hypertension in an infant with double heterozygosity for spondyloepiphyseal dysplasia congenita and achondroplasia
1995
·
Joëlle Günthard
, Christian Fliegel
, et al.
·
Clinical Genetics
·
15
Expression of H-Y antigen in the sex-change fishCoris julis
1983
·
B. J. Ducháč
, E. M. Bühler
·
Cellular and Molecular Life Sciences
·
12
Loss of the Y Chromosome from Bone Marrow Cells of Males with Myeloproliferative Disorders
2009
·
P.E. DiLeo
, H. Müller
, et al.
·
Acta Haematologica
·
11
Possible role of heterochromatin in human aneuploidy
1965
·
G. R. Stalder
, E. M. Buhler
, et al.
·
Human Genetics
·
10
Medical-ethical guidelines for genetic investigations in humans.
1994
·
H J Müller
, Th Deonna
, et al.
·
PubMed
·
7
Fertilität und Turner-Mosaik-Syndrom
1989
·
L. Meyer
, M. Birkhäuser
, et al.
·
Geburtshilfe und Frauenheilkunde
·
7
Acid-phosphatase Activity in Partial Translocation-trisomy
1965
·
G.R. Stalder
, E.M. Buhler
, et al.
·
The Lancet
·
6
Untersuchungen über die Erblichkeit des Isoagglutinintiters
1935
·
E. Bühler
·
Molecular Genetics and Genomics
·
6
Molecular genetic analysis of Turkish cystic fibrosis patients.
1993
·
F F Köprübasi
, N Malik
, et al.
·
PubMed
·
5
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Works count:
45
Citation count:
734
H-index:
16
I10-index:
20
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