Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of multiple phenocopies of unknown origin in a family with ADSNHL

Nelly Abdelfatah , David A McComiskey , Lance Doucette , Anne Griffin
European Journal of Human Genetics 21 ( 10) 1112 -1119

12
2013
A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene

Nelly Abdelfatah , Ahmed A Mostafa , Curtis R French , Lance P Doucette
Human Genetics 1 -15

10
2022
New Syndrome? Robin sequence with facial and digital anomalies in two half‐brothers by the same mother

David Chitayat , Catherine M Meunier , Kathy A Hodgkinson , Michel E Azouz
American journal of medical genetics 40 ( 2) 167 -172

18
1991
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David Chitayat , Kathy A Hodgkinson , Shirley Blaichman , Moy-Fong Chen
American Journal of Medical Genetics 41 49 -51

1991
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David Chitayat , Kathy A Hodgkinson , Moy-Fong Chen , George D Haber
American Journal of Medical Genetics 3236 41 -41

1989
A RETROSPECTIVE ASSESSMENT OF PRENATAL SCREENING TECHNIQUES IN 75 PREGNANCIES RESULTING IN NEURAL-TUBE DEFECTS, AND THE SEQUELAE FOR THE FAMILIES

DN MINECAN , KA HODGKINSON , HJ HOFFMAN , D CHITAYAT
AMERICAN JOURNAL OF HUMAN GENETICS 53 ( 3) 1804 -1804

1993
TRISOMY OF CHROMOSOMES 6P AND 13Q RESULTING FROM A 3-1 SEGREGATION OF A FAMILIAL BALANCED T (6P-3Q) CHROMOSOME REARRANGEMENT

MF CHEN , KA HODGKINSON , D DELNESTE , F TELEJ
AMERICAN JOURNAL OF HUMAN GENETICS 49 ( 4) 258 -258

1991
THE BOR SYNDROME-A CAUSE OF OLIGOHYDRAMNIOS DUE TO RENAL HYPOPLASIA DYSPLASIA

KA HODGKINSON , D CHITAYAT , MP CHEN , GD HABER
AMERICAN JOURNAL OF HUMAN GENETICS 49 ( 4) 140 -140

1991
PATIENTS ATTITUDES TO PRENATAL-DIAGNOSIS FOR APKD

KA HODGKINSON , RG ELLES , EA WATTERS , R HARRIS
JOURNAL OF MEDICAL GENETICS 25 ( 4) 281 -281

1988
Initial clinical manifestations of Arrythmogenic right ventricular cardiomyopathy (ARVC).

M Longley , W McKenna , A Bassett , E Dicks
AMERICAN JOURNAL OF HUMAN GENETICS , 67 (4) p. 114. (2000)

2000
Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) in six Newfoundland families: a sex-limited disease with malignant phenotype in males.

M Longley , S Conners , W McKenna , A Bassett
AMERICAN JOURNAL OF HUMAN GENETICS , 67 (4) p. 114. (2000)

2000
Molecular genetics in the National Health Service in Britain.

R Harris , R Elles , D Craufurd , A Dodge
Journal of Medical Genetics 26 ( 4) 219 -225

16
1989
PREMATURE DEATH IN ADULTS WITH 22Q11. 2 DELETION SYNDROME AND SCHIZOPHRENIA

Anne S Bassett , E Chow , J Husted , K Hodgkinson
SCHIZOPHRENIA BULLETIN 35 119 -119

2009
Drafted for Publication

D Ryan , R Chafe , PC Moorehead , K Hodgkinson
IMPROVING THE TRANSITION FROM PEDIATRIC TO ADULT CARE FOR SURVIVORS OF PEDIATRIC CANCER IN NEWFOUNDLAND, CANADA 3 ( 4) 90 -8

2021
Psychiatric phenotype of a genetic subtype of schizophrenia

AS Bassett , E Chow , L Scutt , K Hodgkinson
Schizophr Res 36 87 -87

4
1999
Recognizing a genetic subtype of schizophrenia.

AS Bassett , E Chow , L Scutt , HM Dorman
MOLECULAR PSYCHIATRY 4 S31 -S31

1
1999
Symptoms of schizophrenia in adults with 22q deletion syndrome.

AS Bassett , E Chow , L Scutt , P AbdelMalik
AMERICAN JOURNAL OF HUMAN GENETICS 67 ( 4) 120 -120

2000
Obstetrical complications in subjects with a genetic subtype of schizophrenia.

HM Dorman , K Hodgkinson , E Chow , LE Scutt
MOLECULAR PSYCHIATRY 4 S33 -S34

1999
Velocardiofacial Syndrome (VCFS) and schizophrenia: A cluster analysis of patients and their dysmorphic features.

L Scutt , S Correia , E Chow , J Hogan
AMERICAN JOURNAL OF HUMAN GENETICS 61 ( 4) A112 -A112

1997