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11 . Academic Journal
Partial maternal heterodisomy of chromosome 17q25 in a case of severe mental retardation
저자
by
Rio, M
;
Ozilou, C
;
Cormier-Daire, V
;
Turleau, C
;
Prieur, M
, et al.
소스
HUMAN GENETICS
; JUN 2001, 108 6, p511-p515, 5p.
Full Text (Springer)
Scopus
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17 . Academic Journal
A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation
저자
by
Colleaux, L
;
Rio, M
;
Heuertz, S
;
Moindrault, S
;
Turleau, C
, et al.
소스
EUROPEAN JOURNAL OF HUMAN GENETICS
; MAY 2001, 9 5, p319-p327, 9p.
Scopus
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17 . Academic Journal
Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann features
저자
by
Fert-Ferrer, S
;
Guichet, A
;
Tantau, J
;
Delezoide, AL
;
Ozilou, C
, et al.
소스
PRENATAL DIAGNOSIS
; JUN 2000, 20 6, p511-p515, 5p.
Scopus
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17 . Academic Journal
Molecular cytogenetic characterization of a new case of partial trisomy 16q24.1-qter: literature review and phenotype-genotype correlations.
저자
by
Brisset, S
;
Joly, G
;
Ozilou, C
;
Lapierre, JM
;
Gosset, P
, et al.
소스
AMERICAN JOURNAL OF HUMAN GENETICS
; OCT 2001, 69 4, p337-p337, 1p. Supplement: 1
Full Text (ScienceDirect)
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17 . Academic Journal
Molecular cytogenetic screening in CHARGE association.
저자
by
Sanlaville, D
;
Lapierre, JM
;
Genevieve, D
;
Ozilou, C
;
Le Lorc'h, M
, et al.
소스
AMERICAN JOURNAL OF HUMAN GENETICS
; OCT 2001, 69 4, p332-p332, 1p. Supplement: 1
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17 . Academic Journal
Two cases of Xq28 functional disomy detected using subtelomeric probes screening.
저자
by
de Blois, MC
;
Sanlaville, D
;
Prieur, M
;
Lapierre, JM
;
Ozilou, C
, et al.
소스
AMERICAN JOURNAL OF HUMAN GENETICS
; OCT 2001, 69 4, p309-p309, 1p. Supplement: 1
Full Text (ScienceDirect)
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17 . Academic Journal
Unbalanced familial cryptic translocation t(8;11) in two fetuses with Beckwith-Wiedemann features.
저자
by
Fert-Ferrer, S
;
Guichet, A
;
Tantau, J
;
Delezoide, AL
;
Ozilou, C
, et al.
소스
AMERICAN JOURNAL OF HUMAN GENETICS
; OCT 1999, 65 4, pA162-pA162, 1p. Supplement: S
Full Text (ScienceDirect)
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17 . Academic Journal
Prenatal diagnosis of GREIG syndrome in a fetus with a de novo translocation t(5;7)(p15;p13).
저자
by
Morichon-Delvallez, N
;
Gosset, P
;
Delezoide, AL
;
Chemouny, S
;
Loison, S
, et al.
소스
AMERICAN JOURNAL OF HUMAN GENETICS
; OCT 1999, 65 4, pA352-pA352, 1p. Supplement: S
Full Text (ScienceDirect)
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