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T Martin-Denavit

Showing results (1-10 of 7) with videos related to

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American Journal of Medical Genetics. Part A|June 24, 2004
Toriello-Carey syndrome and unbalanced translocation t(8;18)(p12;q22)T Martin-Denavit, M Till, H Plauchu
Journal of the European Academy of Dermatology and Venereology : JEADV|March 19, 2022
Cutaneous apocrine adenocarcinoma in a PALB2 germline pathogenic variant carrierS Idoudi, L Golmard, O Harou, et al.
Clinical Genetics|September 13, 2001
Phenotype variability of two FAP families with an identical APC germline mutation at codon 1465: a potential modifier effect?T Martin-Denavit, S Duthel, S Giraud, et al.
Clinical Chemistry|March 3, 1999
Usefulness of procalcitonin in neonates at risk for infectionT Martin-Denavit, G Monneret, J M Labaune, et al.
American Journal of Medical Genetics|October 20, 2000
Ectodermal abnormalities associated with methimazole intrauterine exposureT Martin-Denavit, P Edery, H Plauchu, et al.
Genetic Counseling (Geneva, Switzerland)|January 22, 2005
A new case of a severe clinical phenotype of the cat-eye syndromeT Martin Denavit, V Malan, C Grillon, et al.
Prenatal Diagnosis|July 13, 2002
First prenatal diagnosis of partial trisomy 10 and partial monosomy 15 derived from a maternal translocation (10;15)(q11;q13)T Martin-Denavit, J Attia-Sobol, J Theuil, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|June 24, 2004
Toriello-Carey syndrome and unbalanced translocation t(8;18)(p12;q22)T Martin-Denavit, M Till, H Plauchu
Journal of the European Academy of Dermatology and Venereology : JEADV|March 19, 2022
Cutaneous apocrine adenocarcinoma in a PALB2 germline pathogenic variant carrierS Idoudi, L Golmard, O Harou, et al.
Clinical Genetics|September 13, 2001
Phenotype variability of two FAP families with an identical APC germline mutation at codon 1465: a potential modifier effect?T Martin-Denavit, S Duthel, S Giraud, et al.
Clinical Chemistry|March 3, 1999
Usefulness of procalcitonin in neonates at risk for infectionT Martin-Denavit, G Monneret, J M Labaune, et al.
American Journal of Medical Genetics|October 20, 2000
Ectodermal abnormalities associated with methimazole intrauterine exposureT Martin-Denavit, P Edery, H Plauchu, et al.
Genetic Counseling (Geneva, Switzerland)|January 22, 2005
A new case of a severe clinical phenotype of the cat-eye syndromeT Martin Denavit, V Malan, C Grillon, et al.
Prenatal Diagnosis|July 13, 2002
First prenatal diagnosis of partial trisomy 10 and partial monosomy 15 derived from a maternal translocation (10;15)(q11;q13)T Martin-Denavit, J Attia-Sobol, J Theuil, et al.
Pageof 1