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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 carrier
S 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 infection
T Martin-Denavit, G Monneret, J M Labaune, et al.
American Journal of Medical Genetics
|
October 20, 2000
Ectodermal abnormalities associated with methimazole intrauterine exposure
T 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 syndrome
T 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.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 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 carrier
S 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 infection
T Martin-Denavit, G Monneret, J M Labaune, et al.
American Journal of Medical Genetics
|
October 20, 2000
Ectodermal abnormalities associated with methimazole intrauterine exposure
T 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 syndrome
T 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.
Page
of 1