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R A Pfeiffer

Showing results (31-40 of 205) with videos related to

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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
American Journal of Medical Genetics|June 1, 1983
Acrofacial dysostosis (Nager syndrome): synopsis and report of a new caseR A Pfeiffer, H Stoess
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|April 1, 1983
[The Aase syndrome: hereditary autosomal recessive congenital erythropoiesis insufficiency and triphalangeal thumbs]R A Pfeiffer, E Ambs
Klinische Monatsblatter Fur Augenheilkunde|December 1, 1987
[Short stature, mental retardation, type I preaxial polydactyly with colobomatous abnormalities: a new syndrome]R A Pfeiffer, U Mayer
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|December 1, 1987
[Partial trisomy 1 (1q31-41) caused by intrachromosomal insertion in 1p31.3 in a newborn infant and a sister of the mother]R A Pfeiffer, W Englisch
Human Genetics|July 12, 1978
Balanced and unbalanced pericentric inversion of a chromosome 14R A Pfeiffer, E Kessel
Klinische Padiatrie|January 1, 1991
[Characteristics of a 3-year-old girl with an additional isochromosome of the long arm of an X-chromosome (47,XX, + i(Xq))]R A Pfeiffer, G Wündisch
Annales De Genetique|January 1, 1994
Interstitial deletion 12p13.1-13.3 in a mildly retarded infant with unilateral ectrodactylyU Trautmann, R A Pfeiffer
Pageof 21

Showing results (31-40 of 205) with videos related to

Sort By:
Pageof 21
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
American Journal of Medical Genetics|June 1, 1983
Acrofacial dysostosis (Nager syndrome): synopsis and report of a new caseR A Pfeiffer, H Stoess
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|April 1, 1983
[The Aase syndrome: hereditary autosomal recessive congenital erythropoiesis insufficiency and triphalangeal thumbs]R A Pfeiffer, E Ambs
Klinische Monatsblatter Fur Augenheilkunde|December 1, 1987
[Short stature, mental retardation, type I preaxial polydactyly with colobomatous abnormalities: a new syndrome]R A Pfeiffer, U Mayer
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|December 1, 1987
[Partial trisomy 1 (1q31-41) caused by intrachromosomal insertion in 1p31.3 in a newborn infant and a sister of the mother]R A Pfeiffer, W Englisch
Human Genetics|July 12, 1978
Balanced and unbalanced pericentric inversion of a chromosome 14R A Pfeiffer, E Kessel
Klinische Padiatrie|January 1, 1991
[Characteristics of a 3-year-old girl with an additional isochromosome of the long arm of an X-chromosome (47,XX, + i(Xq))]R A Pfeiffer, G Wündisch
Annales De Genetique|January 1, 1994
Interstitial deletion 12p13.1-13.3 in a mildly retarded infant with unilateral ectrodactylyU Trautmann, R A Pfeiffer
Pageof 21