31

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.

Am J Hum Genet. 1994 Mar;54(3):473-81. Erratum in: Am J Hum Genet 1994 Jul;55(1):217

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32

Normal phenotype with paternal uniparental isodisomy for chromosome 21

Blouin JL, Avramopoulos D, Pangalos C, Antonarakis SE.

Am J Hum Genet. 1993 Nov;53(5):1074-8

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33

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.

Am J Hum Genet. 1992 Nov;51(5):1015-27

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34

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.

Am J Hum Genet. 1992 Dec;51(6):1240-50

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35

Pure partial trisomy of the short arm of chromosome 5

Rethoré MO, Blois MC, Peeters M, Popowski P, Pangalos C, Lejeune J.

Hum Genet. 1989 Jun;82(3):296-8

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36

Genetic counseling in balanced chromosomal inversions

Pangalos C.

J Genet Hum. 1988 Jan;36(1-2):21-31

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37

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.

Am J Hum Genet. 1992 Mar;50(3):544-50

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38

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.

Ann Genet. 1988;31(3):151-4

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39

CFC syndrome: a syndrome distinct from Noonan syndrome

Verloes A, Le Merrer M, Soyeur D, Kaplan J, Pangalos C, Rigo J, Briard ML.

Ann Genet. 1988;31(4):230-4

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40

Ring-14 and trisomy 14q in the same child

Pangalos C, Velissariou V, Ghica M, Liacacos D.

Ann Genet. 1984;27(1):38-40

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41

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

Pangalos C, Couturier J.

Ann Genet. 1981;24(3):179-81

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42

Partial 11q trisomy due to missegregation of maternal t(11;22) (q23;q11.1) translocation (author’s transl)

Pangalos C, Couturier J, Bartsocas C, Theodorou S.

Nouv Presse Med. 1980 Nov 1;9(41):3065-7

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43

Tay-Sachs and Sandhoff diseases: a hypothesis about the primary lesion based on hexosaminidase patterns in interspecific hybrids.

Cong NV, Weil D, Rebourcet R, Pangalos C, Frézal J.

Cytogenet Cell Genet. 1975;14(3-6):442-5

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44

Localization of a structural locus of erythrocyte inorganic pyrophosphatase on chromosome 10 in man by the method of human-hamster cellular hybridization

Van-Cong N, Rebourcet R, Weil D, Pangalos C, Frézal J.

C R Acad Sci Hebd Seances Acad Sci D. 1975 Aug 4-25;281(5-8):435-8

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45

Tay-Sachs and Sandhoff diseases: an hypothesis about the primary lesion based on hexosaminidase patterns in interspecific hybrids

Van Cong N, Weil D, Rebourcet R, Pangalos C, Frézal J.
Birth Defects Orig Artic Ser. 1975;11(3):272-5

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