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Pediatric Cardiology
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March 25, 1999
Resolution of neonatal hypertrophic cardiomyopathy in an infant with an affected mother
B W Eidem, N M Lindor, D J Driscoll
Clinical Dysmorphology
|
January 1, 1996
A neuropsychiatric disorder associated with dense calcification of the external ears and distal muscle wasting: 'Primrose syndrome'
N M Lindor, A D Hoffman, D A Primrose
The Journal of Clinical Endocrinology and Metabolism
|
February 1, 1995
Mutations in the RET protooncogene in sporadic pheochromocytomas
N M Lindor, R Honchel, S Khosla, et al.
Clinical Dysmorphology
|
April 1, 1995
Trisomy 9 mosaicism in a child with a tethered cord
N M Lindor, V V Michels, S Jalal, et al.
Mayo Clinic Proceedings
|
March 22, 2000
von Hippel-Lindau disease
V Couch, N M Lindor, P S Karnes, et al.
Genomics
|
November 24, 1999
Rothmund-thomson syndrome responsible gene, RECQL4: genomic structure and products
S Kitao, N M Lindor, M Shiratori, et al.
American Journal of Medical Genetics
|
September 19, 1997
Melorheostosis in a patient with familial osteopoikilosis
C E Butkus, V V Michels, N M Lindor, et al.
Mayo Clinic Proceedings
|
January 12, 2000
Care of patients and their families with familial adenomatous polyposis
J E King, R R Dozois, N M Lindor, et al.
American Journal of Human Genetics
|
March 23, 2000
Pyogenic arthritis, pyoderma gangrenosum, and acne syndrome maps to chromosome 15q
H B Yeon, N M Lindor, J G Seidman, et al.
Clinical Dysmorphology
|
August 5, 1998
Clinical characteristics associated with dup17(q24q25.1) in a mosaic mother and two non-mosaic daughters
D Babovic-Vuksanovic, J A Westman, S M Jalal, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 59) with videos related to
Sort By:
Page
of 6
Pediatric Cardiology
|
March 25, 1999
Resolution of neonatal hypertrophic cardiomyopathy in an infant with an affected mother
B W Eidem, N M Lindor, D J Driscoll
Clinical Dysmorphology
|
January 1, 1996
A neuropsychiatric disorder associated with dense calcification of the external ears and distal muscle wasting: 'Primrose syndrome'
N M Lindor, A D Hoffman, D A Primrose
The Journal of Clinical Endocrinology and Metabolism
|
February 1, 1995
Mutations in the RET protooncogene in sporadic pheochromocytomas
N M Lindor, R Honchel, S Khosla, et al.
Clinical Dysmorphology
|
April 1, 1995
Trisomy 9 mosaicism in a child with a tethered cord
N M Lindor, V V Michels, S Jalal, et al.
Mayo Clinic Proceedings
|
March 22, 2000
von Hippel-Lindau disease
V Couch, N M Lindor, P S Karnes, et al.
Genomics
|
November 24, 1999
Rothmund-thomson syndrome responsible gene, RECQL4: genomic structure and products
S Kitao, N M Lindor, M Shiratori, et al.
American Journal of Medical Genetics
|
September 19, 1997
Melorheostosis in a patient with familial osteopoikilosis
C E Butkus, V V Michels, N M Lindor, et al.
Mayo Clinic Proceedings
|
January 12, 2000
Care of patients and their families with familial adenomatous polyposis
J E King, R R Dozois, N M Lindor, et al.
American Journal of Human Genetics
|
March 23, 2000
Pyogenic arthritis, pyoderma gangrenosum, and acne syndrome maps to chromosome 15q
H B Yeon, N M Lindor, J G Seidman, et al.
Clinical Dysmorphology
|
August 5, 1998
Clinical characteristics associated with dup17(q24q25.1) in a mosaic mother and two non-mosaic daughters
D Babovic-Vuksanovic, J A Westman, S M Jalal, et al.
Page
of 6