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Journal of Inherited Metabolic Disease
|
May 7, 2005
Selective antibody immune deficiency in a patient with Smith-Lemli-Opitz syndrome
D Babovic-Vuksanovic, R M Jacobson, N M Lindor, et al.
American Journal of Medical Genetics
|
December 31, 1997
De novo 16p deletion: ATR-16 syndrome
N M Lindor, M G Valdes, M Wick, et al.
American Journal of Medical Genetics
|
March 4, 2000
Rothmund-Thomson syndrome due to RECQ4 helicase mutations: report and clinical and molecular comparisons with Bloom syndrome and Werner syndrome
N M Lindor, Y Furuichi, S Kitao, et al.
Annals of Internal Medicine
|
January 15, 1995
Genetic testing in the diagnosis and management of multiple endocrine neoplasia type II
G A Ledger, S Khosla, N M Lindor, et al.
Mayo Clinic Proceedings
|
July 1, 1997
A new autosomal dominant disorder of pyogenic sterile arthritis, pyoderma gangrenosum, and acne: PAPA syndrome
N M Lindor, T M Arsenault, H Solomon, et al.
American Journal of Medical Genetics
|
November 15, 1994
Sanfilippo syndrome type A in two adult sibs
N M Lindor, A Hoffman, J F O'Brien, et al.
Clinical Genetics
|
February 3, 2015
Genetic counselors' practices and confidence regarding variant of uncertain significance results and reclassification from BRCA testing
C L Scherr, N M Lindor, T L Malo, et al.
American Journal of Medical Genetics
|
March 13, 1995
Asplenia in two father-son pairs
N M Lindor, W A Smithson, C A Ahumada, et al.
Mayo Clinic Proceedings
|
January 13, 2001
Application of multicolor fluorescent in situ hybridization for enhanced characterization of chromosomal abnormalities in congenital disorders
S M Jalal, M E Law, N M Lindor, et al.
Neurology
|
July 17, 1999
Familial trigeminal neuralgia and contralateral hemifacial spasm
J M Duff, R J Spinner, N M Lindor, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 59) with videos related to
Sort By:
Page
of 6
Journal of Inherited Metabolic Disease
|
May 7, 2005
Selective antibody immune deficiency in a patient with Smith-Lemli-Opitz syndrome
D Babovic-Vuksanovic, R M Jacobson, N M Lindor, et al.
American Journal of Medical Genetics
|
December 31, 1997
De novo 16p deletion: ATR-16 syndrome
N M Lindor, M G Valdes, M Wick, et al.
American Journal of Medical Genetics
|
March 4, 2000
Rothmund-Thomson syndrome due to RECQ4 helicase mutations: report and clinical and molecular comparisons with Bloom syndrome and Werner syndrome
N M Lindor, Y Furuichi, S Kitao, et al.
Annals of Internal Medicine
|
January 15, 1995
Genetic testing in the diagnosis and management of multiple endocrine neoplasia type II
G A Ledger, S Khosla, N M Lindor, et al.
Mayo Clinic Proceedings
|
July 1, 1997
A new autosomal dominant disorder of pyogenic sterile arthritis, pyoderma gangrenosum, and acne: PAPA syndrome
N M Lindor, T M Arsenault, H Solomon, et al.
American Journal of Medical Genetics
|
November 15, 1994
Sanfilippo syndrome type A in two adult sibs
N M Lindor, A Hoffman, J F O'Brien, et al.
Clinical Genetics
|
February 3, 2015
Genetic counselors' practices and confidence regarding variant of uncertain significance results and reclassification from BRCA testing
C L Scherr, N M Lindor, T L Malo, et al.
American Journal of Medical Genetics
|
March 13, 1995
Asplenia in two father-son pairs
N M Lindor, W A Smithson, C A Ahumada, et al.
Mayo Clinic Proceedings
|
January 13, 2001
Application of multicolor fluorescent in situ hybridization for enhanced characterization of chromosomal abnormalities in congenital disorders
S M Jalal, M E Law, N M Lindor, et al.
Neurology
|
July 17, 1999
Familial trigeminal neuralgia and contralateral hemifacial spasm
J M Duff, R J Spinner, N M Lindor, et al.
Page
of 6