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H D Rott

Showing results (51-60 of 99) with videos related to

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Das Offentliche Gesundheitswesen|February 1, 1981
[Marital conflict in genetic diseases. Attempt at a psychological test objectivization in 48 couples given genetic counseling]H D Rott, H Erzigkeit, K Arnold
Acta Geneticae Medicae Et Gemellologiae|January 1, 1975
[Dermatoglyphics in Noonan's syndrome (author's transl)]H D Rott, G Schwanitz, M Reither
Acta Geneticae Medicae Et Gemellologiae|January 1, 1970
[The importance of cytogenetic studies for the concordance and discordance of twins]G Koch, G Schwanitz, H D Rott
Journal De Genetique Humaine|September 1, 1980
[Situations of conflict among couples demanding genetic counseling]H D Rott, H Erzigkeit, K Arnold
Zeitschrift Fur Kardiologie|July 1, 1976
[Autosomal dominant hereditary atrial septal defect with heart conduction defects and mitral valve insufficiency]A Weikl, H D Rott, E Lang
Human Mutation|October 26, 1999
Mutation screening of the entire coding regions of the TSC1 and the TSC2 gene with the protein truncation test (PTT) identifies frequent splicing defectsK Mayer, W Ballhausen, H D Rott
Lancet (London, England)|January 14, 1984
Duchenne muscular dystrophy: carrier detection by ultrasound and computerised tomographyH D Rott, M Santellani, F H Breimesser
Medizinische Klinik|June 27, 1975
[Chronic renal failure in bourneville-pringle's disease (author's transl)]J F Riemann, M Mörl, H D Rott
Clinical Dysmorphology|January 1, 1995
Specific acromesomelia with facial and renal anomalies: a new syndromeR A Pfeiffer, H Hirschfelder, H D Rott
Zeitschrift Fur Kinderheilkunde|January 1, 1971
[Partial trisonomy C9 in a case of balanced maternal B4-C9 translocation]H D Rott, G Schwanitz, K P Grosse
Pageof 10

Showing results (51-60 of 99) with videos related to

Sort By:
Pageof 10
Das Offentliche Gesundheitswesen|February 1, 1981
[Marital conflict in genetic diseases. Attempt at a psychological test objectivization in 48 couples given genetic counseling]H D Rott, H Erzigkeit, K Arnold
Acta Geneticae Medicae Et Gemellologiae|January 1, 1975
[Dermatoglyphics in Noonan's syndrome (author's transl)]H D Rott, G Schwanitz, M Reither
Acta Geneticae Medicae Et Gemellologiae|January 1, 1970
[The importance of cytogenetic studies for the concordance and discordance of twins]G Koch, G Schwanitz, H D Rott
Journal De Genetique Humaine|September 1, 1980
[Situations of conflict among couples demanding genetic counseling]H D Rott, H Erzigkeit, K Arnold
Zeitschrift Fur Kardiologie|July 1, 1976
[Autosomal dominant hereditary atrial septal defect with heart conduction defects and mitral valve insufficiency]A Weikl, H D Rott, E Lang
Human Mutation|October 26, 1999
Mutation screening of the entire coding regions of the TSC1 and the TSC2 gene with the protein truncation test (PTT) identifies frequent splicing defectsK Mayer, W Ballhausen, H D Rott
Lancet (London, England)|January 14, 1984
Duchenne muscular dystrophy: carrier detection by ultrasound and computerised tomographyH D Rott, M Santellani, F H Breimesser
Medizinische Klinik|June 27, 1975
[Chronic renal failure in bourneville-pringle's disease (author's transl)]J F Riemann, M Mörl, H D Rott
Clinical Dysmorphology|January 1, 1995
Specific acromesomelia with facial and renal anomalies: a new syndromeR A Pfeiffer, H Hirschfelder, H D Rott
Zeitschrift Fur Kinderheilkunde|January 1, 1971
[Partial trisonomy C9 in a case of balanced maternal B4-C9 translocation]H D Rott, G Schwanitz, K P Grosse
Pageof 10