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Brigitte H. W. Faas et al.
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Giuseppe Merla et al.
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Narrowing candidate region for monosomy 9p syndrome to a 4.7-Mb segment at 9p22.2-p23
H Kawara et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2006)
Dissection of molecular mechanisms underlying speech and language disorders
SE Fisher
APPLIED PSYCHOLINGUISTICS (2005)
Detection of large-scale variation in the human genome
AJ Iafrate et al.
NATURE GENETICS (2004)
Diverse fates of paralogs following segmental duplication of telomeric genes
A Wong et al.
GENOMICS (2004)
Genitourinary phenotype in XX patients with distal 9p monosomy
Y Fujimoto et al.
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Molecular rulers for calibrating phenotypic effects of telomere imbalance
CL Martin et al.
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Female gonadal development in XX patients with distal 9p monosomy
T Ogata et al.
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The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome
L Crisponi et al.
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The SPCH1 region on human 7q31: Genomic characterization of the critical interval and localization of translocations associated with speech and language disorder
CSL Lai et al.
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Sex-determining gene(s) on distal 9p: Clinical and molecular studies in six cases
K Muroya et al.
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