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1 . Academic Journal
Holoprosencephaly and ZIC2 microdeletions: novel clinical and epidemiological specificities delineated.
저자
by
Chabchoub, E
;
Willekens, D
;
Vermeesch, JR
;
Fryns, J-P
.
소스
Clinical Genetics
. Jun2012, Vol. 81 Issue 6, p584-589. 6p. 1 Color Photograph, 1 Chart.
Web of Science
Scopus
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6 . Academic Journal
Preimplantation genetic diagnosis using fluorescent in situ hybridization for cancer predisposition syndromes caused by microdeletions
저자
by
Vanneste, E
;
Melotte, C
;
Debrock, S
;
D’Hooghe, T
;
Brems, H
, et al.
소스
Human Reproduction
. Jun 01, 2009 24(6):1522-1528
Full Text (OUP)
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7 .
Current Controversies in Prenatal Diagnosis 3: Gene editing should replace embryo selection following PGD
저자
by
Wells, D
;
Vermeesch, JR
;
Simpson, JL
.
소스
Prenatal diagnosis
. 39(5)
Open Access (OpenAIRE)
Scopus
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5 . Academic Journal
Ring syndrome caused by ring chromosome 7 without loss of subtelomeric sequences.
저자
by
Vermeesch, JR
;
Baten, E
;
Fryns, J-P
;
Devriendt, K
.
소스
Clinical Genetics
. Nov2002, Vol. 62 Issue 5, p415-417. 3p.
Web of Science
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6 .
Cryptic deletions are a common finding in 'balanced' reciprocal and complex chromosome rearrangements: a study of 59 cases
저자
by
DE GREGORI, M
;
Ciccone, R
;
Magini, P
;
Pramparo, T
;
Gimelli, S
, et al.
소스
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7 . Academic Journal
Contiguous gene deletion within chromosome arm 10q is associated with juvenile polyposis of infancy, reflecting cooperation between the BMPR1A and PTEN tumor-suppressor genes
저자
by
Delnatte, C
;
Sanlaville, D
;
Mougenot, JF
;
Vermeesch, JR
;
Houdayer, C
, et al.
소스
AMERICAN JOURNAL OF HUMAN GENETICS
; JUN 2006, 78 6, p1066-p1074, 9p.
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7 . Academic Journal
Molecular pathogenesis of multiple gastrointestinal stromal tumors in NF1 patients
저자
by
Maertens, O
;
Prenen, H
;
Wozniak, A
;
Sciot, R
;
Pauwels, P
, et al.
소스
HUMAN MOLECULAR GENETICS
; MAR 15 2006, 15 6, p1015-p1023, 9p.
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7 . Academic Journal
Single-cell chromosomal imbalances detection by array CGH
저자
by
Le Caignec, C
;
Spits, C
;
Sermon, K
;
De Rycke, M
;
Thienpont, B
, et al.
소스
NUCLEIC ACIDS RESEARCH
; 2006, 34 9, pe68 12p.
Open Access (OUP)
Scopus
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7 . Academic Journal
Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC
저자
by
Liehr, T
;
Starke, H
;
Senger, G
;
Melotte, C
;
Weise, A
, et al.
소스
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
; JAN 1 2006, 140A 1, p46-p51, 6p.
Scopus
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7 . Academic Journal
Small supernumerary marker chromosomes progress towards a genotype-phenotype correlation
저자
by
Liehr, T
;
Mrasek, K
;
Weise, A
;
Dufke, A
;
Rodriguez, L
, et al.
소스
CYTOGENETIC AND GENOME RESEARCH
; 2006, 112 1-2, p23-p34, 12p.
Scopus
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