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N M Lindor

Showing results (21-30 of 59) with videos related to

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American Journal of Medical Genetics|October 6, 1999
CALL gene is haploinsufficient in a 3p- syndrome patientD Angeloni, N M Lindor, S Pack, et al.
American Journal of Medical Genetics|December 18, 1998
Visual impairment due to macular disciform scars in a 20-year-old man with Smith-Magenis syndrome: another ophthalmologic complicationD Babovic-Vuksanovic, S M Jalal, J A Garrity, et al.
American Journal of Medical Genetics|March 15, 1994
Screening the dystrophin gene suggests a high rate of polymorphism in general but no exonic deletions in schizophrenicsN M Lindor, J L Sobell, L L Heston, et al.
Clinical Genetics|June 4, 1998
Maternal cell contamination of buccal smear samples in nursing neonatesD Babovic-Vuksanovic, V V Michels, M E Law, et al.
The British Journal of Dermatology|June 20, 2002
Progressive extensive osteoma cutis associated with dysmorphic features: a new syndrome? Case report and review of the literatureM D P Davis, M R Pittelkow, N M Lindor, et al.
Clinical Genetics|October 1, 1993
Mosaic trisomy 16 in a thriving infant: maternal heterodisomy for chromosome 16N M Lindor, S M Jalal, S N Thibodeau, et al.
Nature Genetics|May 13, 1999
Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndromeS Kitao, A Shimamoto, M Goto, et al.
American Journal of Medical Genetics|June 19, 1995
Central pontine myelinolysis as a complication of partial ornithine carbamoyl transferase deficiencyL R Mattson, N M Lindor, D H Goldman, et al.
Mayo Clinic Proceedings|May 1, 1997
Genetic testing in medullary thyroid carcinoma syndromes: mutation types and clinical significanceH M Heshmati, H Gharib, S Khosla, et al.
Mayo Clinic Proceedings|August 1, 1992
A genetic review of complete and partial hydatidiform moles and nonmolar triploidyN M Lindor, J A Ney, T A Gaffey, et al.
Pageof 6

Showing results (21-30 of 59) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics|October 6, 1999
CALL gene is haploinsufficient in a 3p- syndrome patientD Angeloni, N M Lindor, S Pack, et al.
American Journal of Medical Genetics|December 18, 1998
Visual impairment due to macular disciform scars in a 20-year-old man with Smith-Magenis syndrome: another ophthalmologic complicationD Babovic-Vuksanovic, S M Jalal, J A Garrity, et al.
American Journal of Medical Genetics|March 15, 1994
Screening the dystrophin gene suggests a high rate of polymorphism in general but no exonic deletions in schizophrenicsN M Lindor, J L Sobell, L L Heston, et al.
Clinical Genetics|June 4, 1998
Maternal cell contamination of buccal smear samples in nursing neonatesD Babovic-Vuksanovic, V V Michels, M E Law, et al.
The British Journal of Dermatology|June 20, 2002
Progressive extensive osteoma cutis associated with dysmorphic features: a new syndrome? Case report and review of the literatureM D P Davis, M R Pittelkow, N M Lindor, et al.
Clinical Genetics|October 1, 1993
Mosaic trisomy 16 in a thriving infant: maternal heterodisomy for chromosome 16N M Lindor, S M Jalal, S N Thibodeau, et al.
Nature Genetics|May 13, 1999
Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndromeS Kitao, A Shimamoto, M Goto, et al.
American Journal of Medical Genetics|June 19, 1995
Central pontine myelinolysis as a complication of partial ornithine carbamoyl transferase deficiencyL R Mattson, N M Lindor, D H Goldman, et al.
Mayo Clinic Proceedings|May 1, 1997
Genetic testing in medullary thyroid carcinoma syndromes: mutation types and clinical significanceH M Heshmati, H Gharib, S Khosla, et al.
Mayo Clinic Proceedings|August 1, 1992
A genetic review of complete and partial hydatidiform moles and nonmolar triploidyN M Lindor, J A Ney, T A Gaffey, et al.
Pageof 6