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R A Pfeiffer

Showing results (61-70 of 205) with videos related to

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Journal De Genetique Humaine|March 1, 1979
[Familial translocation 22/Y and partial autosomal trisomy in a young girl]E Kessel, R A Pfeiffer, P Welling
Klinische Padiatrie|May 1, 1976
[The phenotype of the trisomy of the short arm of chromosome no. 4. (a new case with t (4p; 11q) (author's transl)]E Kessel, R A Pfeiffer, W Kosenow
Klinische Padiatrie|January 1, 1980
[Postaxial polydactyly: a symptom of partial trisomy of the long arm of chromosome 13. Two new observations with 46, XX, t (22;13) (q13;q31) and 46, XY, Dup (13) (pter-q34::q22-qter) (author's transl)]E Kessel, R A Pfeiffer, C Baisch
Pediatric Radiology|January 1, 1992
An autosomal recessive variant of spondylo-epiphyseal dysplasia in three sibsR A Pfeiffer, J Suess, M Haagen
The Journal of Pediatrics|December 1, 1977
A syndrome of short stature, amimic facies, enamel hypoplasia, slowly progressive stiffness of the joints and high-pitched voice in two siblingsR A Pfeiffer, D Palm, W Teller
Helvetica Paediatrica Acta|September 1, 1977
[The Schwartz-Jampel syndrome (myotonia chondrodystrophica)]R A Pfeiffer, H Bauer, C Petersen
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Genetic counseling of cleft sternumD Kotzot, W Huk, R A Pfeiffer
Clinical Genetics|December 1, 1994
Single mandibular incisor in a patient with del (18p) anomalyR A Pfeiffer, K Hertrich, M Cohen
European Journal of Pediatrics|January 1, 1987
An unusual, possibly "new" MA/MR syndrome with sagittal craniosynostosisR A Pfeiffer, U Tietze, W Welte
Journal of Medical Genetics|February 1, 1977
46,XX/46,XX,r(15) mosaiciam: report of a caseR A Pfeiffer, R Dhadial, W Lenz
Pageof 21

Showing results (61-70 of 205) with videos related to

Sort By:
Pageof 21
Journal De Genetique Humaine|March 1, 1979
[Familial translocation 22/Y and partial autosomal trisomy in a young girl]E Kessel, R A Pfeiffer, P Welling
Klinische Padiatrie|May 1, 1976
[The phenotype of the trisomy of the short arm of chromosome no. 4. (a new case with t (4p; 11q) (author's transl)]E Kessel, R A Pfeiffer, W Kosenow
Klinische Padiatrie|January 1, 1980
[Postaxial polydactyly: a symptom of partial trisomy of the long arm of chromosome 13. Two new observations with 46, XX, t (22;13) (q13;q31) and 46, XY, Dup (13) (pter-q34::q22-qter) (author's transl)]E Kessel, R A Pfeiffer, C Baisch
Pediatric Radiology|January 1, 1992
An autosomal recessive variant of spondylo-epiphyseal dysplasia in three sibsR A Pfeiffer, J Suess, M Haagen
The Journal of Pediatrics|December 1, 1977
A syndrome of short stature, amimic facies, enamel hypoplasia, slowly progressive stiffness of the joints and high-pitched voice in two siblingsR A Pfeiffer, D Palm, W Teller
Helvetica Paediatrica Acta|September 1, 1977
[The Schwartz-Jampel syndrome (myotonia chondrodystrophica)]R A Pfeiffer, H Bauer, C Petersen
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Genetic counseling of cleft sternumD Kotzot, W Huk, R A Pfeiffer
Clinical Genetics|December 1, 1994
Single mandibular incisor in a patient with del (18p) anomalyR A Pfeiffer, K Hertrich, M Cohen
European Journal of Pediatrics|January 1, 1987
An unusual, possibly "new" MA/MR syndrome with sagittal craniosynostosisR A Pfeiffer, U Tietze, W Welte
Journal of Medical Genetics|February 1, 1977
46,XX/46,XX,r(15) mosaiciam: report of a caseR A Pfeiffer, R Dhadial, W Lenz
Pageof 21