Pangalos C - Search Results

1

Ring-14 and trisomy 14q in the same child.

Pangalos C, Velissariou V, Ghica M, Liacacos D. Pangalos C, et al. Ann Genet. 1984;27(1):38-40. Ann Genet. 1984. PMID: 6609671

2

[Molecular analysis of the parental origin of trisomy in two families with two children having regular trisomy 21].

Pangalos C, Serre JL, Ghica M, Abazis D, Sinet PM, Rethoré MO, Lejeune J. Pangalos C, et al. Ann Genet. 1988;31(3):151-4. Ann Genet. 1988. PMID: 2851959 French.

3

Pure partial trisomy of the short arm of chromosome 5.

Rethoré MO, Blois MC, Peeters M, Popowski P, Pangalos C, Lejeune J. Rethoré MO, et al. Among authors: pangalos c. Hum Genet. 1989 Jun;82(3):296-8. doi: 10.1007/BF00291177. Hum Genet. 1989. PMID: 2731942

4

CFC syndrome: a syndrome distinct from Noonan syndrome.

Verloes A, Le Merrer M, Soyeur D, Kaplan J, Pangalos C, Rigo J, Briard ML. Verloes A, et al. Among authors: pangalos c. Ann Genet. 1988;31(4):230-4. Ann Genet. 1988. PMID: 3265306

5

Partial trisomy 13 (q21.3 leads to qter) resulting from a maternal translocation t (13;21).

Pangalos C, Couturier J. Pangalos C, et al. Ann Genet. 1981;24(3):179-81. Ann Genet. 1981. PMID: 6974532 No abstract available.

6

Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis.

Pangalos C, Avramopoulos D, Blouin JL, Raoul O, deBlois MC, Prieur M, Schinzel AA, Gika M, Abazis D, Antonarakis SE. Pangalos C, et al. Am J Hum Genet. 1994 Mar;54(3):473-81. Am J Hum Genet. 1994. PMID: 8116616 Free PMC article.

7

No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21.

Pangalos C, Théophile D, Sinet PM, Marks A, Stamboulieh-Abazis D, Chettouh Z, Prieur M, Verellen C, Rethoré MO, Lejeune J, et al. Pangalos C, et al. Am J Hum Genet. 1992 Dec;51(6):1240-50. Am J Hum Genet. 1992. PMID: 1463008 Free PMC article.

8

Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: case report and review of the literature on partial trisomy 17qter.

Sarri C, Gyftodimou J, Avramopoulos D, Grigoriadou M, Pedersen W, Pandelia E, Pangalos C, Abazis D, Kitsos G, Vassilopoulos D, Brøndum-Nielsen K, Petersen MB. Sarri C, et al. Among authors: pangalos c. Am J Med Genet. 1997 May 2;70(1):87-94. doi: 10.1002/(sici)1096-8628(19970502)70:1<87::aid-ajmg16>3.0.co;2-t. Am J Med Genet. 1997. PMID: 9129747 Review.

9

DNA polymorphism analysis in families with recurrence of free trisomy 21.

Pangalos CG, Talbot CC Jr, Lewis JG, Adelsberger PA, Petersen MB, Serre JL, Rethoré MO, de Blois MC, Parent P, Schinzel AA, et al. Pangalos CG, et al. Am J Hum Genet. 1992 Nov;51(5):1015-27. Am J Hum Genet. 1992. PMID: 1415248 Free PMC article.

10

The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms.

Antonarakis SE, Petersen MB, McInnis MG, Adelsberger PA, Schinzel AA, Binkert F, Pangalos C, Raoul O, Slaugenhaupt SA, Hafez M, et al. Antonarakis SE, et al. Among authors: pangalos c. Am J Hum Genet. 1992 Mar;50(3):544-50. Am J Hum Genet. 1992. PMID: 1347192 Free PMC article.

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