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ZFA. Zeitschrift Fur Allgemeinmedizin
|
June 10, 1981
[Prenatal examinations. Indications and informative value]
G Schwanitz
Fortschritte Der Kieferorthopadie
|
April 1, 1989
[Consultation for patients with cheilognathopalatoschisis and their family members. Cooperation between orthodontists and human geneticists]
G Schwanitz, S Zschiesche
Roczniki Akademii Medycznej W Bialymstoku (1995)
|
December 20, 2005
Application of specific cytologic, cytogenetic and molecular-cytogenetic techniques for the characterization of solid tumors
G Schwanitz, R Raff
MMW, Munchener Medizinische Wochenschrift
|
October 24, 1975
[Contribution to information and genetic counseling in Mekkel's syndrome (author's transl)]
G Koch, G Schwanitz
Annales De Genetique
|
January 1, 1987
Partial monosomy 22 as result of an X/22 translocation in a newborn with DiGeorge syndrome
G Schwanitz, K Zerres
Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1978
Double trisomy as a mosaic. Case history (48, XYY, + 21/47,XY, +21) and survey of the literature of mixed autosomal-gonosomal trisomies
G Schwanitz, M Hagner
Annales De Genetique
|
January 1, 1984
[Phenotype signs at different ages in partial trisomy 3p by familial translocation 3/5]
G Schwanitz, K Zerres
Deutsche Medizinische Wochenschrift (1946)
|
January 14, 1972
[Chromosome studies after chronic benzol exposure]
G Hartwich, G Schwanitz
Klinische Padiatrie
|
May 1, 1975
[Report on a variant of the fetal-face-syndrome with acral dysostosis (Robinow-Silverman-Smith-Syndrome) (author's transl)]
H Hanssler, G Schwanitz
Folia Humanistica
|
January 1, 1985
[Not Available]
G Koch, G Schwanitz
Page
of 13
Search research articles
Search
Showing results (1-10 of 123) with videos related to
Sort By:
Page
of 13
ZFA. Zeitschrift Fur Allgemeinmedizin
|
June 10, 1981
[Prenatal examinations. Indications and informative value]
G Schwanitz
Fortschritte Der Kieferorthopadie
|
April 1, 1989
[Consultation for patients with cheilognathopalatoschisis and their family members. Cooperation between orthodontists and human geneticists]
G Schwanitz, S Zschiesche
Roczniki Akademii Medycznej W Bialymstoku (1995)
|
December 20, 2005
Application of specific cytologic, cytogenetic and molecular-cytogenetic techniques for the characterization of solid tumors
G Schwanitz, R Raff
MMW, Munchener Medizinische Wochenschrift
|
October 24, 1975
[Contribution to information and genetic counseling in Mekkel's syndrome (author's transl)]
G Koch, G Schwanitz
Annales De Genetique
|
January 1, 1987
Partial monosomy 22 as result of an X/22 translocation in a newborn with DiGeorge syndrome
G Schwanitz, K Zerres
Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1978
Double trisomy as a mosaic. Case history (48, XYY, + 21/47,XY, +21) and survey of the literature of mixed autosomal-gonosomal trisomies
G Schwanitz, M Hagner
Annales De Genetique
|
January 1, 1984
[Phenotype signs at different ages in partial trisomy 3p by familial translocation 3/5]
G Schwanitz, K Zerres
Deutsche Medizinische Wochenschrift (1946)
|
January 14, 1972
[Chromosome studies after chronic benzol exposure]
G Hartwich, G Schwanitz
Klinische Padiatrie
|
May 1, 1975
[Report on a variant of the fetal-face-syndrome with acral dysostosis (Robinow-Silverman-Smith-Syndrome) (author's transl)]
H Hanssler, G Schwanitz
Folia Humanistica
|
January 1, 1985
[Not Available]
G Koch, G Schwanitz
Page
of 13