Citation: H. Chen et Se. Antonarakis, THE SH3D1A GENE MAPS TO HUMAN-CHROMOSOME 21Q22.1-]Q22.2, Cytogenetics and cell genetics, 78(3-4), 1997, pp. 213-215
Authors:
ANTONARAKIS SE
CHEN HM
LALIOTI MD
SCOTT HS
CHRAST R
BLOUIN JL
MITTAZ L
GUIDI S
PAOLINIGIACOBINO A
ROSSIER C
Citation: Se. Antonarakis et al., PROGRESS TOWARD THE TRANSCRIPTION MAP OF HUMAN-CHROMOSOME-21 AND INITIAL CHARACTERIZATION OF SEVERAL OF ITS GENES, Cytogenetics and cell genetics, 77, 1997, pp. 12-12
Authors:
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DAGNABRICARELLI F
BASSO G
ANTONARAKIS SE
CHESSELS J
COTTER F
NIZETIC D
Citation: Jh. Ives et al., AN INITIAL COMPARATIVE-STUDY OF GENE-EXPRESSION LEVELS IN DOWN-SYNDROME LEUKEMIC AND NORMAL CLINICAL-SAMPLES, Cytogenetics and cell genetics, 77, 1997, pp. 31-31
Authors:
DOMBROSKI BA
TON CC
NATH S
CHAKRAVARTI A
LASSETER VK
SNYDER SE
WOLYNIEC P
NESTADT G
ANTONARAKIS SE
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LUEBBERT H
HOUSMAN D
KAZAZIAN HH
PULVER AE
Citation: Ba. Dombroski et al., A SUSCEPTIBILITY LOCUS FOR SCHIZOPHRENIA ON CHROMOSOME 8P, American journal of medical genetics, 74(6), 1997, pp. 668-668
Authors:
KARAYIORGOU M
GALKE B
BUDARF M
NESTADT G
ANTONARAKIS SE
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Citation: M. Karayiorgou et al., FURTHER CHARACTERIZATION OF THE 22Q11 SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, American journal of medical genetics, 74(6), 1997, pp. 677-677
Authors:
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BLOUIN JL
MEHENNI H
MEHTA TY
SHETH FJ
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Citation: U. Radhakrishna et al., THE GENE FOR AUTOSOMAL-DOMINANT HIDROTIC ECTODERMAL DYSPLASIA (CLOUSTON-SYNDROME) IN A LARGE INDIAN FAMILY MAPS TO THE 13Q11-Q12.1 PERICENTROMERIC REGION, American journal of medical genetics, 71(1), 1997, pp. 80-86
Authors:
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MORRIS MA
DAHOUNHADORN S
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Citation: S. Eliez et al., FAMILIAL TRANSLOCATION T(Y-15)(Q12-P11) AND DE-NOVO DELETION OF THE PRADER-WILLI-SYNDROME (PWS) CRITICAL REGION ON 15Q11-Q13, American journal of medical genetics, 70(3), 1997, pp. 222-228
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BOTTANI A
MEDEIROS PFV
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SCHINZEL A
Citation: S. Fokstuen et al., LARYNGEAL ATRESIA TYPE-III (GLOTTIC WEB) WITH 22Q11.2 MICRODELETION -REPORT OF 3 PATIENTS, American journal of medical genetics, 70(2), 1997, pp. 130-133
Citation: Ps. Knoepfler et al., MEIS1 AND PKNOX1 BIND DNA COOPERATIVELY WITH PBX1 UTILIZING AN INTERACTION SURFACE DISRUPTED IN ONCOPROTEIN E2A-PBX1, Proceedings of the National Academy of Sciences of the United Statesof America, 94(26), 1997, pp. 14553-14558
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MEHENNI H
BLOUIN JL
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Citation: H. Mehenni et al., PEUTZ-JEGHERS-SYNDROME - CONFIRMATION OF LINKAGE TO CHROMOSOME 19P13.3 AND IDENTIFICATION OF A POTENTIAL 2ND LOCUS, ON 19Q13.4, American journal of human genetics, 61(6), 1997, pp. 1327-1334
Authors:
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PAPASAVVAS MP
VELCULESCU VE
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ROSSIER C
ANTONARAKIS SE
Citation: Hs. Scott et al., A GLOBAL COMPARISON OF GENE-EXPRESSION PATTERNS BETWEEN DOWN-SYNDROMEAND NORMAL-CELLS BY SERIAL ANALYSIS OF GENE-EXPRESSION, American journal of human genetics, 61(4), 1997, pp. 207-207
Authors:
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SCOTT HS
BURESI C
ROSSIER C
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MALAFOSSE A
ANTONARAKIS SE
Citation: Md. Lalioti et al., DODECAMER REPEAT EXPANSION IN THE CYSTATIN-B GENE IN PROGRESSIVE MYOCLONUS EPILEPSY (EPM1), American journal of human genetics, 61(4), 1997, pp. 272-272
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MEHENNI H
BLOUIN JL
RADHAKRISHNA U
BARADWAJ S
BARADWAJ K
DIXIT VB
RICHARDS KF
FENOLL BA
LEAL AS
RAVAL RC
ANTONARAKIS SE
Citation: H. Mehenni et al., PEUTZ-JEGHERS-SYNDROME - CONFIRMATION OF LINKAGE TO CHROMOSOME 19P13.3 AND IDENTIFICATION OF A POTENTIAL 2ND LOCUS ON 19Q13.4, American journal of human genetics, 61(4), 1997, pp. 402-402
Authors:
DAHOUN S
KERN I
SANDO Z
ANTONARAKIS SE
SAKKAS D
MORRIS MA
Citation: S. Dahoun et al., FAMILIAL T(6-21)(P21.1-P13) TRANSLOCATION RETAINING AG-NORS ASSOCIATED WITH MALE-STERILITY, American journal of human genetics, 61(4), 1997, pp. 687-687
Authors:
BLOUIN JL
SAIL GD
ROSSIER C
ANTONARAKIS SE
Citation: Jl. Blouin et al., A SPECIFIC CHROMOSOME 21Q22.1 EXON TRAPPING FOR DETECTION OF EXPRESSED SEQUENCES WITHIN A GENE-RICH REGION, American journal of human genetics, 61(4), 1997, pp. 958-958
Citation: Hm. Chen et al., CHROMOSOME 21CEN CONTAINS A TESTIS-EXPRESSED GENE ENCODING A PROTEIN WITH TRANSMEMBRANE, TYROSINE PHOSPHATASE, AND TENSIN DOMAINS AND HAS HOMOLOGOUS COPIES ON CHROMOSOME-13, CHROMOSOME-15, CHROMOSOME-22, AND CHROMOSOME-Y, American journal of human genetics, 61(4), 1997, pp. 965-965
Citation: R. Chrast et al., LINEARIZATION AND PURIFICATION OF BAC CLONES FOR TG MICE GENERATION, American journal of human genetics, 61(4), 1997, pp. 967-967
Authors:
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BLOUIN JL
SAIL GD
ROSSIER C
ANTONARAKIS SE
SCOTT HS
Citation: S. Guidi et al., ISOLATION AND CHARACTERIZATION OF A NOVEL HUMAN-CHROMOSOME 21Q22 GENE(C21ORF1), AND ITS MOUSE AND CHICKEN HOMOLOGS, American journal of human genetics, 61(4), 1997, pp. 996-996
Authors:
NAGAMINE K
KUDOH J
KAWASAKI K
ASAKAWA S
ABE I
MINOSHIMA S
SCOTT HS
ANTONARAKIS SE
ITO F
SHIMIZU N
Citation: K. Nagamine et al., EXON TRAPPING, CDNA CLONING, AND GENOMIC SEQUENCING OF THE APECED REGION OF CHROMOSOME 21Q22.3, American journal of human genetics, 61(4), 1997, pp. 1673-1673
Authors:
PULVER AE
ANTONARAKIS SE
BLOUIN JL
GEHRIG C
RADHAKVISHNA U
LOETSCHER E
KAZAZIAN HH
DOMBROSKI B
LASSETER VK
NESTADT G
NATH S
CHAKRAVARTI A
DEMARCHI N
HOUSMAN D
WOLYNIEC P
Citation: Ae. Pulver et al., A GENOME SEARCH FOR SCHIZOPHRENIA SUSCEPTIBILITY LOCI - SIB-PAIR SHARING OF ALLELES ON CHROMOSOME 5Q22-5Q31 IN 54 PEDIGREES, American journal of human genetics, 61(4), 1997, pp. 1701-1701
Authors:
MITTAZ L
SCOTT HS
NIZETIC D
ANTONARAKIS SE
Citation: L. Mittaz et al., EDITING OF GLUTAMATE-RECEPTOR PRE-MESSENGER-RNAS IN TRISOMY-21 FETAL BRAIN - EVIDENCE FOR IN-VIVO SUBSTRATES OF HRED1 AND IMPLICATIONS FOR THE DOWN-SYNDROME PHENOTYPES, American journal of human genetics, 61(4), 1997, pp. 1842-1842
Authors:
NEERMANARBEZ M
ANTONARAKIS SE
BLOUIN JL
ZEINALI S
AKHTARI M
AFSHAR Y
TUDDENHAM EGD
Citation: M. Neermanarbez et al., THE LOCUS FOR COMBINED FACTOR-V FACTOR-VIII DEFICIENCY (F5F8D) MAPS TO 18Q21, BETWEEN D18S849 AND D18S1103, American journal of human genetics, 61(1), 1997, pp. 143-150