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Results: 1-9 |
Results: 9

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

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

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

Authors: BRZUSTOWICZ LM HONER WG CHOW EWC HOGAN J HODGKINSON K BASSETT AS
Citation: Lm. Brzustowicz et al., USE OF A QUANTITATIVE TRAIT TO MAP A LOCUS ASSOCIATED WITH SEVERITY OF POSITIVE SYMPTOMS IN FAMILIAL SCHIZOPHRENIA TO CHROMOSOME 6P, American journal of human genetics, 61(6), 1997, pp. 1388-1396

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

Authors: BRZUSTOWICZ LM HONER WG CHOW EWC HOGAN J HODGKINSON K SCUTT L BASSETT AS
Citation: Lm. Brzustowicz et al., QUANTITATIVE SYMPTOM MEASURES LINKED TO CHROMOSOME 6P IN A CANADIAN SAMPLE OF FAMILIAL SCHIZOPHRENIA, American journal of human genetics, 61(4), 1997, pp. 1568-1568

Authors: BUSHER H HODGKINSON K
Citation: H. Busher et K. Hodgkinson, COOPERATION AND TENSION BETWEEN AUTONOMOUS SCHOOLS - A STUDY OF INTER-SCHOOL NETWORKING, Educational review, 48(1), 1996, pp. 55-64

Authors: CHITAYAT D HODGKINSON K LUKE A WINSOR E ROSE T KALOUSEK D
Citation: D. Chitayat et al., PRENATAL-DIAGNOSIS AND FETOPATHOLOGICAL FINDINGS IN 5 FETUSES WITH TRISOMY-9, American journal of medical genetics, 56(3), 1995, pp. 247-251

Authors: CHITAYAT D MOORE L DELBIGIO MR MACGREGOR D BENZEEV B HODGKINSON K DECK J STOTHERS T RITCHIE S TOI A
Citation: D. Chitayat et al., FAMILIAL DANDY-WALKER MALFORMATION ASSOCIATED WITH MACROCEPHALY, FACIAL ANOMALIES, DEVELOPMENTAL DELAY, AND BRAIN-STEM DYSGENESIS - PRENATAL-DIAGNOSIS AND POSTNATAL OUTCOME IN BROTHERS - A NEW SYNDROME, American journal of medical genetics, 52(4), 1994, pp. 406-415
Risultati: 1-9 |