SANTESSON B - Search Results

1

Malformation syndrome in man associated with triploidy (69 chromosomes).

BOOK JA, SANTESSON B. BOOK JA, et al. Among authors: santesson b. Lancet. 1960 Apr 16;1(7129):858-9. doi: 10.1016/s0140-6736(60)90737-6. Lancet. 1960. PMID: 13802657 No abstract available.

2

Malformation syndrome associated with triploidy--further chromosome studies of the patient and his family.

BOOK JA, MASTERSON JG, SANTESSON B. BOOK JA, et al. Among authors: santesson b. Acta Genet Stat Med. 1962;12:193-201. doi: 10.1159/000151198. Acta Genet Stat Med. 1962. PMID: 13968911 No abstract available.

3

Karyotyping human amnitic-fluid cels.

Santesson B, Akesson HO, Böök JA, Brosset A. Santesson B, et al. Lancet. 1969 Nov 15;2(7629):1067-8. doi: 10.1016/s0140-6736(69)90664-3. Lancet. 1969. PMID: 4187557 No abstract available.

4

[Sex chromatin and its clinical significance].

BOOK JA, SANTESSON B. BOOK JA, et al. Among authors: santesson b. Sven Lakartidn. 1962 Jan 18;59:159-74. Sven Lakartidn. 1962. PMID: 13871126 Swedish. No abstract available.

5

Chromosome and chromatid-type aberrations induced by Cobalt 60 irradiation and tritiated uridine in human leukocyte cultures.

Lindahl-Kiessling K, Santesson B, Böök JA. Lindahl-Kiessling K, et al. Among authors: santesson b. Chromosoma. 1970;31(3):280-4. doi: 10.1007/BF00321224. Chromosoma. 1970. PMID: 5489361 No abstract available.

6

Karyotypes of cultured cells from foetal membranes of normal newborns.

Böök JA, Kjessler B, Santesson B. Böök JA, et al. Among authors: santesson b. J Med Genet. 1968 Sep;5(3):224-6. doi: 10.1136/jmg.5.3.224. J Med Genet. 1968. PMID: 5708028 Free PMC article. No abstract available.

7

The mortality of human XO embryos.

Santesson B, BOOK JA, Kjessler B. Santesson B, et al. J Reprod Fertil. 1973 Jul;34(1):51-5. doi: 10.1530/jrf.0.0340051. J Reprod Fertil. 1973. PMID: 4737074 No abstract available.

8

DNA synthesis of human XYY cells. Autoradiography and fluorescence pattern.

Santesson B, Böök JA, Gustavson KH. Santesson B, et al. Clin Genet. 1972;3(1):73-81. doi: 10.1111/j.1399-0004.1972.tb01729.x. Clin Genet. 1972. PMID: 5013869 No abstract available.

9

Three non-mongoloid patients of similar phenotype with an extra G-like chromosome.

Gustavson KH, Hitrec V, Santesson B. Gustavson KH, et al. Among authors: santesson b. Clin Genet. 1972;3(2):135-46. doi: 10.1111/j.1399-0004.1972.tb01735.x. Clin Genet. 1972. PMID: 5054315 No abstract available.

10

Male pseudohermaphroditism with 45X-46XYq- mosaicism in a pair of monozygotic twins.

Bengtsson B, Gustavson KH, Reuterskiöld G, Santesson B, Ahnsén S. Bengtsson B, et al. Among authors: santesson b. Clin Genet. 1974;5(2):133-43. doi: 10.1111/j.1399-0004.1974.tb01675.x. Clin Genet. 1974. PMID: 4857285 No abstract available.

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