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de la CHAPELLE

Showing results (61-70 of 603) with videos related to

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Cell|November 1, 1978
Recessive sex-determining genes in human XX male syndromeA de la Chapelle, G C Koo, S S Wachtel
Human Genetics|June 30, 1977
Clozapine-induced agranulocytosis. A genetic and epidemiologic studyA de la Chapelle, C Kari, M Nurminen, et al.
Human Genetics|November 1, 1993
A rare reciprocal translocation (12;21) segregating for nine generationsS Koskinen, T Onnelainen, A de la Chapelle, et al.
Nature|July 5, 1987
Exchange of terminal portions of X- and Y-chromosomal short arms in human XX malesD C Page, L G Brown, A de la Chapelle
The EMBO Journal|February 1, 1990
An interspersed repeated sequence specific for human subtelomeric regionsF Rouyer, A de la Chapelle, M Andersson, et al.
Scandinavian Journal of Immunology|September 1, 1975
Massive invasion of fetal lymphocytes into the mother's blood at induced abortionR Zilliacus, A de la Chapelle, J Schröder, et al.
Blood|November 1, 1987
Molecular characterization of chromosome 7 long arm deletions in myeloid disordersJ Kere, T Ruutu, R Lahtinen, et al.
Clinical Genetics|March 1, 1990
Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial resultsH Kääriäinen, M Lindlöf, H Somer, et al.
Reproduction, Nutrition, Development|January 1, 1990
The etiology of XX sex reversalA de la Chapelle, J Hästbacka, T Korhonen, et al.
Clinical Genetics|September 1, 1987
X-linked retinoschisis is closely linked to DXS41 and DXS16 but not DXS85T Alitalo, J Kärnä, H Forsius, et al.
Pageof 61

Showing results (61-70 of 603) with videos related to

Sort By:
Pageof 61
Cell|November 1, 1978
Recessive sex-determining genes in human XX male syndromeA de la Chapelle, G C Koo, S S Wachtel
Human Genetics|June 30, 1977
Clozapine-induced agranulocytosis. A genetic and epidemiologic studyA de la Chapelle, C Kari, M Nurminen, et al.
Human Genetics|November 1, 1993
A rare reciprocal translocation (12;21) segregating for nine generationsS Koskinen, T Onnelainen, A de la Chapelle, et al.
Nature|July 5, 1987
Exchange of terminal portions of X- and Y-chromosomal short arms in human XX malesD C Page, L G Brown, A de la Chapelle
The EMBO Journal|February 1, 1990
An interspersed repeated sequence specific for human subtelomeric regionsF Rouyer, A de la Chapelle, M Andersson, et al.
Scandinavian Journal of Immunology|September 1, 1975
Massive invasion of fetal lymphocytes into the mother's blood at induced abortionR Zilliacus, A de la Chapelle, J Schröder, et al.
Blood|November 1, 1987
Molecular characterization of chromosome 7 long arm deletions in myeloid disordersJ Kere, T Ruutu, R Lahtinen, et al.
Clinical Genetics|March 1, 1990
Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial resultsH Kääriäinen, M Lindlöf, H Somer, et al.
Reproduction, Nutrition, Development|January 1, 1990
The etiology of XX sex reversalA de la Chapelle, J Hästbacka, T Korhonen, et al.
Clinical Genetics|September 1, 1987
X-linked retinoschisis is closely linked to DXS41 and DXS16 but not DXS85T Alitalo, J Kärnä, H Forsius, et al.
Pageof 61