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A Pfeiffer

Showing results (71-80 of 1,039) with videos related to

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Analytical Chemistry|July 29, 2017
On-Chip Photothermal Analyte Detection Using Integrated Luminescent Temperature SensorsSimon A Pfeiffer, Stefan Nagl
Journal of Medical Genetics|October 1, 1982
Congenital universal alopecia, mental deficiency, and microcephaly in two sibsR A Pfeiffer, J Völklein
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|October 1, 1984
[Phenotype of trisomy 9]R A Pfeiffer, R Müller
Ophthalmic Paediatrics and Genetics|April 1, 1985
Familial congenital cataract, non-progressive neurological disorders and mental deficiency: a new X-linked syndrome?R A Pfeiffer, J Steffann
Monatsschrift Fur Kinderheilkunde|July 1, 1971
[Forms of intersexuality in X0-XY-mosaicism]H Stolecke, R A Pfeiffer
Zeitschrift Fur Kinderheilkunde|January 1, 1971
[Agenesia of the tibia, duplication of the fibula and mirror foot (diplopodia) in mother and child]R A Pfeiffer, M Roeskau
Human Genetics|November 1, 1979
Tandem duplication (5q13 to 22) in a mentally deficient girlE Kessel, R A Pfeiffer
Zeitschrift Fur Kinderheilkunde|October 1, 1973
[Ectrodactyly, ectodermal dysplasia, and cleft lip and palate: an hereditary syndrome with an autosomal dominant mode of inheritance (author's transl)]R A Pfeiffer, C Verbeck
Die Quintessenz Der Zahntechnik|June 1, 1990
[Adaptation of completely dentulous subjects to various designs of palatal coverage]K M Lehmann, A Pfeiffer
Human Heredity|January 1, 1984
Evidence that activities of coagulation factors VII and X are linked to chromosome 13 (q34)R Ott, R A Pfeiffer
Pageof 104

Showing results (71-80 of 1,039) with videos related to

Sort By:
Pageof 104
Analytical Chemistry|July 29, 2017
On-Chip Photothermal Analyte Detection Using Integrated Luminescent Temperature SensorsSimon A Pfeiffer, Stefan Nagl
Journal of Medical Genetics|October 1, 1982
Congenital universal alopecia, mental deficiency, and microcephaly in two sibsR A Pfeiffer, J Völklein
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|October 1, 1984
[Phenotype of trisomy 9]R A Pfeiffer, R Müller
Ophthalmic Paediatrics and Genetics|April 1, 1985
Familial congenital cataract, non-progressive neurological disorders and mental deficiency: a new X-linked syndrome?R A Pfeiffer, J Steffann
Monatsschrift Fur Kinderheilkunde|July 1, 1971
[Forms of intersexuality in X0-XY-mosaicism]H Stolecke, R A Pfeiffer
Zeitschrift Fur Kinderheilkunde|January 1, 1971
[Agenesia of the tibia, duplication of the fibula and mirror foot (diplopodia) in mother and child]R A Pfeiffer, M Roeskau
Human Genetics|November 1, 1979
Tandem duplication (5q13 to 22) in a mentally deficient girlE Kessel, R A Pfeiffer
Zeitschrift Fur Kinderheilkunde|October 1, 1973
[Ectrodactyly, ectodermal dysplasia, and cleft lip and palate: an hereditary syndrome with an autosomal dominant mode of inheritance (author's transl)]R A Pfeiffer, C Verbeck
Die Quintessenz Der Zahntechnik|June 1, 1990
[Adaptation of completely dentulous subjects to various designs of palatal coverage]K M Lehmann, A Pfeiffer
Human Heredity|January 1, 1984
Evidence that activities of coagulation factors VII and X are linked to chromosome 13 (q34)R Ott, R A Pfeiffer
Pageof 104