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Results: 1-25 | 26-50 | 51-56
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DELINEATING A 22Q11 DELETION SUBTYPE OF SCHIZOPHRENIA
Authors: SCUTT L CORREIA S CHOW E HOGAN J HODGKINSON K JONES C HONER W KAEGI S WEKSBERG R BASSETT AS
Citation: L. Scutt et al., DELINEATING A 22Q11 DELETION SUBTYPE OF SCHIZOPHRENIA, Schizophrenia research, 29(1-2), 1998, pp. 131-131
22Q-11.2 DELETION SYNDROME AND SCHIZOPHRENIA
Authors: BASSETT A HODGKINSON K CHOW E SCUTT L WEKSBERG R
Citation: A. Bassett et al., 22Q-11.2 DELETION SYNDROME AND SCHIZOPHRENIA, Schizophrenia research, 29(1-2), 1998, pp. 131-131
22Q11 DELETION SYNDROME IN ADULTS WITH SCHIZOPHRENIA
Authors: BASSETT AS HODGKINSON K CHOW EWC CORREIA S SCUTT LE WEKSBERG R
Citation: As. Bassett et al., 22Q11 DELETION SYNDROME IN ADULTS WITH SCHIZOPHRENIA, American journal of medical genetics, 81(4), 1998, pp. 328-337
INTRODUCTION TO OVERGROWTH SYNDROMES
Authors: NERI G COHEN MM WEKSBERG R
Citation: G. Neri et al., INTRODUCTION TO OVERGROWTH SYNDROMES, American journal of medical genetics, 79(4), 1998, pp. 233-233
MOLECULAR-GENETICS OF WIEDEMANN-BECKWITH-SYNDROME
Authors: LI M SQUIRE JA WEKSBERG R
Citation: M. Li et al., MOLECULAR-GENETICS OF WIEDEMANN-BECKWITH-SYNDROME, American journal of medical genetics, 79(4), 1998, pp. 253-259
SCHIMKE IMMUNOOSSEOUS DYSPLASIA COMPLICATED BY MOYAMOYA PHENOMENON
Authors: BOERKOEL CF NOWACZYK MJM BLASER SI MESCHINO WS WEKSBERG R
Citation: Cf. Boerkoel et al., SCHIMKE IMMUNOOSSEOUS DYSPLASIA COMPLICATED BY MOYAMOYA PHENOMENON, American journal of medical genetics, 78(2), 1998, pp. 118-122
MRI FINDINGS IN MACROCEPHALY-CUTIS MARMORATA TELANGIECTATICA CONGENITA
Authors: CARCAO M BLASER SI GRANT RM WEKSBERG R SIEGELBARTELT J
Citation: M. Carcao et al., MRI FINDINGS IN MACROCEPHALY-CUTIS MARMORATA TELANGIECTATICA CONGENITA, American journal of medical genetics, 76(2), 1998, pp. 165-167
OVERGROWTH SYNDROMES AND GENOMIC IMPRINTING - FROM MOUSE TO MAN
Authors: LI M SQUIRE JA WEKSBERG R
Citation: M. Li et al., OVERGROWTH SYNDROMES AND GENOMIC IMPRINTING - FROM MOUSE TO MAN, Clinical genetics, 53(3), 1998, pp. 165-170
EXAMPLE OF SOMATIC MOSAICISM IN A SERIES OF DE-NOVO NEUROFIBROMATOSISTYPE-1 CASES DUE TO A MATERNALLY DERIVED DELETION
Authors: AINSWORTH PJ CHAKRABORTY PK WEKSBERG R
Citation: Pj. Ainsworth et al., EXAMPLE OF SOMATIC MOSAICISM IN A SERIES OF DE-NOVO NEUROFIBROMATOSISTYPE-1 CASES DUE TO A MATERNALLY DERIVED DELETION, Human mutation, 9(5), 1997, pp. 452-457
VELOCARDIOFACIAL SYNDROME (VCFS) IN SCHIZOPHRENIA - COGNITIVE FEATURES
Authors: BURY AS CHOW EWC WEKSBERG R CORREIA S SCUTT L BASSETT AS
Citation: As. Bury et al., VELOCARDIOFACIAL SYNDROME (VCFS) IN SCHIZOPHRENIA - COGNITIVE FEATURES, Schizophrenia research, 24(1-2), 1997, pp. 53-53
VELO-CARDIO-FACIAL SYNDROME - A TRUE GENETIC SUBTYPE OF SCHIZOPHRENIA
Authors: HODGKINSON KA CHOW E CORREIA S SCUTT L MCALDUFF J BEATTY B SQUIRE J WEKSBERG R BASSETT AS
Citation: Ka. Hodgkinson et al., VELO-CARDIO-FACIAL SYNDROME - A TRUE GENETIC SUBTYPE OF SCHIZOPHRENIA, Schizophrenia research, 24(1-2), 1997, pp. 53-53
MAPPING OF THE GENE ENCODING THE INTEGRIN-LINKED KINASE, ILK, TO HUMAN-CHROMOSOME 11P15.5-P15.4
Authors: HANNIGAN GE BAYANI J WEKSBERG R BEATTY B PANDITA A DEDHAR S SQUIRE J
Citation: Ge. Hannigan et al., MAPPING OF THE GENE ENCODING THE INTEGRIN-LINKED KINASE, ILK, TO HUMAN-CHROMOSOME 11P15.5-P15.4, Genomics, 42(1), 1997, pp. 177-179
MACROCEPHALY-CUTIS MARMORATA TELANGIECTATICA CONGENITA - A DISTINCT DISORDER WITH DEVELOPMENTAL DELAY AND CONNECTIVE-TISSUE ABNORMALITIES
Authors: MOORE CA TORIELLO HV ABUELO DN BULL MJ CURRY CJR HALL BD HIGGINS JV STEVENS CA TWERSKY S WEKSBERG R DOBYNS WB
Citation: Ca. Moore et al., MACROCEPHALY-CUTIS MARMORATA TELANGIECTATICA CONGENITA - A DISTINCT DISORDER WITH DEVELOPMENTAL DELAY AND CONNECTIVE-TISSUE ABNORMALITIES, American journal of medical genetics, 70(1), 1997, pp. 67-73
RELAXATION OF IMPRINTING OF HUMAN INSULIN-LIKE-GROWTH-FACTOR-II GENE,IGF2, IN SPORADIC BREAST CARCINOMAS
Authors: WU HK SQUIRE JA CATZAVELOS CG WEKSBERG R
Citation: Hk. Wu et al., RELAXATION OF IMPRINTING OF HUMAN INSULIN-LIKE-GROWTH-FACTOR-II GENE,IGF2, IN SPORADIC BREAST CARCINOMAS, Biochemical and biophysical research communications, 235(1), 1997, pp. 123-129
PROMOTER-DEPENDENT TISSUE-SPECIFIC EXPRESSIVE NATURE OF IMPRINTING GENE, INSULIN-LIKE GROWTH-FACTOR-II, IN HUMAN TISSUES
Authors: WU HK SQUIRE JA SONG QL WEKSBERG R
Citation: Hk. Wu et al., PROMOTER-DEPENDENT TISSUE-SPECIFIC EXPRESSIVE NATURE OF IMPRINTING GENE, INSULIN-LIKE GROWTH-FACTOR-II, IN HUMAN TISSUES, Biochemical and biophysical research communications, 233(1), 1997, pp. 221-226
LOSS OF IMPRINTING OF HUMAN INSULIN-LIKE-GROWTH-FACTOR-II GENE, IGF2,IN ACUTE MYELOID-LEUKEMIA
Authors: WU HK WEKSBERG R MINDEN MD SQUIRE JA
Citation: Hk. Wu et al., LOSS OF IMPRINTING OF HUMAN INSULIN-LIKE-GROWTH-FACTOR-II GENE, IGF2,IN ACUTE MYELOID-LEUKEMIA, Biochemical and biophysical research communications, 231(2), 1997, pp. 466-472
TREATABLE PSYCHIATRIC-DISORDERS IN WILLIAMS-SYNDROME
Authors: CORREIA S WEKSBERG R COSTA T HODGKINSON KA BASSETT AS
Citation: S. Correia et al., TREATABLE PSYCHIATRIC-DISORDERS IN WILLIAMS-SYNDROME, American journal of human genetics, 61(4), 1997, pp. 527-527
IS THERE A SUBTYPE OF SCHIZOPHRENIA ASSOCIATED WITH A CHROMOSOME 22Q11 DELETION AND VELOCARDIOFACIAL SYNDROME
Authors: HODGKINSON KA CORREIA S SCUTT L CHOW E WEKSBERG R BASSETT A
Citation: Ka. Hodgkinson et al., IS THERE A SUBTYPE OF SCHIZOPHRENIA ASSOCIATED WITH A CHROMOSOME 22Q11 DELETION AND VELOCARDIOFACIAL SYNDROME, American journal of human genetics, 61(4), 1997, pp. 565-565
VELOCARDIOFACIAL SYNDROME (VCFS) AND SCHIZOPHRENIA - A CLUSTER-ANALYSIS OF PATIENTS AND THEIR DYSMORPHIC FEATURES
Authors: SCUTT L CORREIA S CHOW E HOGAN J JONES C HODGKINSON K KAEGI S WEKSBERG R BASSETT AS
Citation: L. Scutt et al., VELOCARDIOFACIAL SYNDROME (VCFS) AND SCHIZOPHRENIA - A CLUSTER-ANALYSIS OF PATIENTS AND THEIR DYSMORPHIC FEATURES, American journal of human genetics, 61(4), 1997, pp. 632-632
BECKWITH-WIEDEMANN-SYNDROME - UNIPARENTAL DISOMY AND TUMOR-DEVELOPMENT
Authors: WEKSBERG R NELSON R SHUMAN C YANLING F SQUIRE J
Citation: R. Weksberg et al., BECKWITH-WIEDEMANN-SYNDROME - UNIPARENTAL DISOMY AND TUMOR-DEVELOPMENT, American journal of human genetics, 61(4), 1997, pp. 1889-1889
GLYPICANS - A GROWING TREND
Authors: WEKSBERG R SQUIRE JA TEMPLETON DM
Citation: R. Weksberg et al., GLYPICANS - A GROWING TREND, Nature genetics, 12(3), 1996, pp. 225-227
GENOMIC IMPRINTING IN TUMORS
Authors: SQUIRE J WEKSBERG R
Citation: J. Squire et R. Weksberg, GENOMIC IMPRINTING IN TUMORS, Seminars in cancer biology, 7(1), 1996, pp. 41-47
FISH DETECTION OF CHROMOSOME-15 DELETIONS IN PRADER-WILLI AND ANGELMAN SYNDROMES (VOL 62, PG 216, 1996)
Authors: TESHIMA I CHADWICK D CHITAYAT D KOBAYASHI J RAY P SHUMAN C SIEGELBARTELT J STRASBERG P WEKSBERG R
Citation: I. Teshima et al., FISH DETECTION OF CHROMOSOME-15 DELETIONS IN PRADER-WILLI AND ANGELMAN SYNDROMES (VOL 62, PG 216, 1996), American journal of medical genetics, 64(3), 1996, pp. 527-527
FISH DETECTION OF CHROMOSOME-15 DELETIONS IN PRADER-WILLI AND ANGELMAN SYNDROMES
Authors: TESHIMA I CHADWICK D CHITAYAT D KOBAYASHI J RAY P SHUMAN C SIEGELBARTELT J STRASBERG P WEKSBERG R
Citation: I. Teshima et al., FISH DETECTION OF CHROMOSOME-15 DELETIONS IN PRADER-WILLI AND ANGELMAN SYNDROMES, American journal of medical genetics, 62(3), 1996, pp. 216-223
MOLECULAR-BIOLOGY OF BECKWITH-WIEDEMANN SYNDROME
Authors: WEKSBERG R SQUIRE JA
Citation: R. Weksberg et Ja. Squire, MOLECULAR-BIOLOGY OF BECKWITH-WIEDEMANN SYNDROME, Medical and pediatric oncology, 27(5), 1996, pp. 462-469
Risultati: 1-25 | 26-50 | 51-56