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American Journal of Medical Genetics. Part A
|
April 23, 2004
Maternal UPD(14) in the patient with a normal karyotype: clinical report and a systematic search for cases in samples sent for testing for Prader-Willi syndrome
Helen Cox, H Bullman, I K Temple
Journal of Medical Genetics
|
December 1, 1990
Dilemmas in counselling: the EEC syndrome
K Tse, I K Temple, M Baraitser
Journal of Medical Genetics
|
December 10, 2002
Transient neonatal diabetes, a disorder of imprinting
I K Temple, J P H Shield
Pediatric Diabetes
|
March 16, 2004
Neonatal diabetes mellitus
J P H Shield, I K Temple
Clinical Dysmorphology
|
August 24, 1999
Anterior chamber eye anomalies, redundant skin and syndactyly--a new syndrome associated with breakpoints at 2q37.2 and 7q36.3
I K Temple, C Browne, P Hodgkins
Journal of Medical Genetics
|
December 1, 1988
Congenital spinal deformity in a three generation family
I K Temple, T G Thomas, M Baraitser
Journal of Medical Genetics
|
October 3, 1999
A probable case of familial Weaver syndrome associated with neoplasia
C Derry, I K Temple, K Venkat-Raman
Clinical Dysmorphology
|
October 1, 1995
Absent iris stroma, narrow body build and small facial bones: a new association or variant of SHORT syndrome?
A Bankier, C G Keith, I K Temple
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1994
Association of atrial-ventricular septal defect, blepharophimosis, anal and radial defects in sibs: a new syndrome?
R S Houlston, R Ironton, I K Temple
American Journal of Medical Genetics
|
April 14, 1997
Coloboma, mental retardation, hypogonadism, and obesity: critical review of the so-called Biemond syndrome type 2, updated nosology, and delineation of three "new" syndromes
A Verloes, I K Temple, S Bonnet, et al.
Page
of 10
Search research articles
Search
Showing results (11-20 of 99) with videos related to
Sort By:
Page
of 10
American Journal of Medical Genetics. Part A
|
April 23, 2004
Maternal UPD(14) in the patient with a normal karyotype: clinical report and a systematic search for cases in samples sent for testing for Prader-Willi syndrome
Helen Cox, H Bullman, I K Temple
Journal of Medical Genetics
|
December 1, 1990
Dilemmas in counselling: the EEC syndrome
K Tse, I K Temple, M Baraitser
Journal of Medical Genetics
|
December 10, 2002
Transient neonatal diabetes, a disorder of imprinting
I K Temple, J P H Shield
Pediatric Diabetes
|
March 16, 2004
Neonatal diabetes mellitus
J P H Shield, I K Temple
Clinical Dysmorphology
|
August 24, 1999
Anterior chamber eye anomalies, redundant skin and syndactyly--a new syndrome associated with breakpoints at 2q37.2 and 7q36.3
I K Temple, C Browne, P Hodgkins
Journal of Medical Genetics
|
December 1, 1988
Congenital spinal deformity in a three generation family
I K Temple, T G Thomas, M Baraitser
Journal of Medical Genetics
|
October 3, 1999
A probable case of familial Weaver syndrome associated with neoplasia
C Derry, I K Temple, K Venkat-Raman
Clinical Dysmorphology
|
October 1, 1995
Absent iris stroma, narrow body build and small facial bones: a new association or variant of SHORT syndrome?
A Bankier, C G Keith, I K Temple
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1994
Association of atrial-ventricular septal defect, blepharophimosis, anal and radial defects in sibs: a new syndrome?
R S Houlston, R Ironton, I K Temple
American Journal of Medical Genetics
|
April 14, 1997
Coloboma, mental retardation, hypogonadism, and obesity: critical review of the so-called Biemond syndrome type 2, updated nosology, and delineation of three "new" syndromes
A Verloes, I K Temple, S Bonnet, et al.
Page
of 10