Gilgenkrantz S - Search Results

1

Proximal trisomy 13. A family with balanced reciprocal translocation t(8;13) in seven members and Robertsonian translocation t(13;14) in three members.

Gilgenkrantz S, Defeche C, Stehlin S, Gregoire MJ. Gilgenkrantz S, et al. Hum Genet. 1981;58(4):436-40. doi: 10.1007/BF00282833. Hum Genet. 1981. PMID: 7327568

2

[Union of 2 carriers of a balanced translocation. Familial study of 3 generations].

Gilgenkrantz S, Grégoire MJ, Chery M, Defèche C. Gilgenkrantz S, et al. Ann Genet. 1985;28(3):164-6. Ann Genet. 1985. PMID: 3879150 French.

3

Congenital acute lymphoblastic leukemia with chromosomal abnormalities including a translocation (1;4;22).

Gilgenkrantz S, Benz E, Chiclet AM, Buisine J, Gregoire MJ, Olive D, Vinet E, Streiff F. Gilgenkrantz S, et al. Cancer Genet Cytogenet. 1983 Sep;10(1):37-42. doi: 10.1016/0165-4608(83)90103-6. Cancer Genet Cytogenet. 1983. PMID: 6576852

4

Duplication 15q22 to 15qter and its phenotypic expression.

Gregoire MJ, Boue J, Junien C, Pernot C, Gilgenkrantz S, Zergollern L. Gregoire MJ, et al. Among authors: gilgenkrantz s. Hum Genet. 1981;59(4):429-33. doi: 10.1007/BF00295485. Hum Genet. 1981. PMID: 7333596 No abstract available.

5

Partial proximal trisomy of the long arm of chromosome 5 (q13 leads to q22) resulting from maternal insertion der ins (10;5).

Gilgenkrantz S, Dulucq P, Bresson JL, Gouget A, Pernot C, Gregoire MJ. Gilgenkrantz S, et al. J Med Genet. 1981 Dec;18(6):465-9. doi: 10.1136/jmg.18.6.465. J Med Genet. 1981. PMID: 7334508 Free PMC article.

6

[Translocation (3;20) and anorchism].

Gilgenkrantz S, Cruz-Marin F, Gregoire MJ, Walter S, Pierson M. Gilgenkrantz S, et al. J Genet Hum. 1981 Sep;29(3):321-7. J Genet Hum. 1981. PMID: 7334352 French. No abstract available.

7

[Cytogenetic studies in spontaneous abortions].

Gilgenkrantz S, Gregoire MJ, Streiff F. Gilgenkrantz S, et al. Bull Assoc Anat (Nancy). 1976 Jun;60(169):357-65. Bull Assoc Anat (Nancy). 1976. PMID: 1021170 French.

8

Sublocalisation of the X breakpoint in the translocation (X; 18)(p11.2; q11.2) primary change in synovial sarcomas.

Gilgenkrantz S, Chery M, Teboul M, Mujica P, Leotard B, Gregoire MJ, Boman F, Duprez A, Hanauer A. Gilgenkrantz S, et al. Oncogene. 1990 Jul;5(7):1063-6. Oncogene. 1990. PMID: 2165233

9

Association of del(11)(p15.1p12), aniridia, catalase deficiency, and cardiomyopathy.

Gilgenkrantz S, Vigneron C, Gregoire MJ, Pernot C, Raspiller A. Gilgenkrantz S, et al. Am J Med Genet. 1982 Sep;13(1):39-49. doi: 10.1002/ajmg.1320130108. Am J Med Genet. 1982. PMID: 6127950

10

[Mental retardation and fragile X chromosome. Clinical and cytogenetic study of 3 families].

Gilgenkrantz S, Boué J, Grégoire MJ, Tejada I. Gilgenkrantz S, et al. J Genet Hum. 1984 Jul;32(3):199-207. J Genet Hum. 1984. PMID: 6481342 French.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

229 results

Search Page

Filters