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Results: 1-11 |
Results: 11
A DUPLICATION ON CHROMOSOME 22Q11 IS THE BASIS FOR THE COMMON DELETION THAT OCCURS IN VELO-CARDIO-FACIAL SYNDROME PATIENTS
Authors: MORROW BE EDELMANN L FERREIRA J PANDITA RK CARLSON CG PROCTER JE JACKSON M WILSON D GOLDBERG R SHPRINTZEN R KUCHERLAPATI R
Citation: Be. Morrow et al., A DUPLICATION ON CHROMOSOME 22Q11 IS THE BASIS FOR THE COMMON DELETION THAT OCCURS IN VELO-CARDIO-FACIAL SYNDROME PATIENTS, American journal of human genetics, 61(4), 1997, pp. 25-25
MOLECULAR DEFINITION OF 22Q11 DELETIONS IN 151 VELO-CARDIO-FACIAL-SYNDROME PATIENTS
Authors: CARLSON C SIROTKIN H PANDITA R GOLDBERG R MCKIE J WADEY R PATANJALI SR WEISSMAN SM ANYANEYEBOA K WARBURTON D SCAMBLER P SHPRINTZEN R KUCHERLAPATI R MORROW BE
Citation: C. Carlson et al., MOLECULAR DEFINITION OF 22Q11 DELETIONS IN 151 VELO-CARDIO-FACIAL-SYNDROME PATIENTS, American journal of human genetics, 61(3), 1997, pp. 620-629
MOLECULAR ANALYSIS OF VELO-CARDIO-FACIAL SYNDROME PATIENTS WITH PSYCHIATRIC-DISORDERS
Authors: CARLSON C PAPOLOS D PANDITA RK FAEDDA GL VEIT S GOLDBERG R SHPRINTZEN R KUCHERLAPATI R MORROW B
Citation: C. Carlson et al., MOLECULAR ANALYSIS OF VELO-CARDIO-FACIAL SYNDROME PATIENTS WITH PSYCHIATRIC-DISORDERS, American journal of human genetics, 60(4), 1997, pp. 851-859
ISOLATION OF A NEW CLATHRIN HEAVY-CHAIN GENE WITH MUSCLE-SPECIFIC EXPRESSION FROM THE REGION COMMONLY DELETED IN VELO-CARDIO-FACIAL SYNDROME
Authors: SIROTKIN H MORROW B DASGUPTA R GOLDBERG R PATANJALI SR SHI GP CANNIZZARO L SHPRINTZEN R WEISSMAN SM KUCHERIAPATI R
Citation: H. Sirotkin et al., ISOLATION OF A NEW CLATHRIN HEAVY-CHAIN GENE WITH MUSCLE-SPECIFIC EXPRESSION FROM THE REGION COMMONLY DELETED IN VELO-CARDIO-FACIAL SYNDROME, Human molecular genetics, 5(5), 1996, pp. 617-624
ASSOCIATION OF CODON-108 158 CATECHOL-O-METHYLTRANSFERASE GENE POLYMORPHISM WITH THE PSYCHIATRIC MANIFESTATIONS OF VELO-CARDIO-FACIAL SYNDROME/
Authors: LACHMAN HM MORROW B SHPRINTZEN R VEIT S PARSIA SS FAEDDA G GOLDBERG R KUCHERLAPATI R PAPOLOS DF
Citation: Hm. Lachman et al., ASSOCIATION OF CODON-108 158 CATECHOL-O-METHYLTRANSFERASE GENE POLYMORPHISM WITH THE PSYCHIATRIC MANIFESTATIONS OF VELO-CARDIO-FACIAL SYNDROME/, American journal of medical genetics, 67(5), 1996, pp. 468-472
ASSOCIATION OF SCHIZOPHRENIA WITH VCFS AND 22Q11 DELETIONS
Authors: MORROW BE SIROTKIN H GOLDBERG R CARLSON C SHPRINTZEN R KUCHERLAPATI R
Citation: Be. Morrow et al., ASSOCIATION OF SCHIZOPHRENIA WITH VCFS AND 22Q11 DELETIONS, Biological psychiatry, 39(7), 1996, pp. 139-139
HEMIMAXILLOFACIAL DYSPLASIA - A REPORT OF 2 NEW CASES AND FURTHER DELINEATION OF THE DISORDER
Authors: EISIG S MARION R SHPRINTZEN R SHANSKE AL
Citation: S. Eisig et al., HEMIMAXILLOFACIAL DYSPLASIA - A REPORT OF 2 NEW CASES AND FURTHER DELINEATION OF THE DISORDER, American journal of human genetics, 57(4), 1995, pp. 478-478
MOLECULAR DEFINITION OF 22Q11 DELETIONS IN VELO-CARDIO-FACIAL SYNDROME
Authors: MORROW B GOLDBERG R CARLSON C SIROTKIN H SHPRINTZEN R KUCHERLAPATI R
Citation: B. Morrow et al., MOLECULAR DEFINITION OF 22Q11 DELETIONS IN VELO-CARDIO-FACIAL SYNDROME, American journal of human genetics, 57(4), 1995, pp. 1428-1428
MOLECULAR DEFINITION OF THE 22Q11 DELETIONS IN VELO-CARDIO-FACIAL SYNDROME
Authors: MORROW B GOLDBERG R CARLSON C DASGUPTA R SIROTKIN H COLLINS J DUNHAM I ODONNELL H SCAMBLER P SHPRINTZEN R KUCHERLAPATI R
Citation: B. Morrow et al., MOLECULAR DEFINITION OF THE 22Q11 DELETIONS IN VELO-CARDIO-FACIAL SYNDROME, American journal of human genetics, 56(6), 1995, pp. 1391-1403
SCHIZOPHRENIA AND CHROMOSOMAL DELETIONS WITHIN 22Q11.2
Authors: LINDSAY EA MORRIS MA GOS A NESTADT G WOLYNIEC PS LASSETER VK SHPRINTZEN R ANTONARAKIS SE BALDINI A PULVER AE
Citation: Ea. Lindsay et al., SCHIZOPHRENIA AND CHROMOSOMAL DELETIONS WITHIN 22Q11.2, American journal of human genetics, 56(6), 1995, pp. 1502-1503
VARIABLE PHENOTYPES IN VELOCARDIOFACIAL SYNDROME WITH CHROMOSOMAL DELETION
Authors: MOTZKIN B MARION R GOLDBERG R SHPRINTZEN R SAENGER P
Citation: B. Motzkin et al., VARIABLE PHENOTYPES IN VELOCARDIOFACIAL SYNDROME WITH CHROMOSOMAL DELETION, The Journal of pediatrics, 123(3), 1993, pp. 406-410
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