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American Journal of Medical Genetics. Part A
|
September 27, 2014
Inverted duplication with deletion: first interstitial case suggesting a novel undescribed mechanism of formation
J Milosevic, L El Khattabi, A Roubergue, et al.
Prenatal Diagnosis
|
March 12, 1999
Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature
L Faivre, N Morichon-Delvallez, G Viot, et al.
Journal of Medical Genetics
|
October 4, 2002
Homozygosity mapping of a Dyggve-Melchior-Clausen syndrome gene to chromosome 18q21.1
C Thauvin-Robinet, V El Ghouzzi, W Chemaitilly, et al.
Gynecologie, Obstetrique, Fertilite & Senologie
|
February 15, 2020
[Adverse obstetric and perinatal outcome with in vitro fertilization technology: A French nationwide population-based study]
F Pessione, J De Mouzon, A Deveaux, et al.
Clinical Genetics
|
January 11, 2016
Complex mode of inheritance in holoprosencephaly revealed by whole exome sequencing
C Mouden, C Dubourg, W Carré, et al.
The Journal of Pediatrics
|
July 11, 2001
Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome
H De Leersnyder, M C De Blois, B Claustrat, et al.
Prenatal Diagnosis
|
June 22, 2000
Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann features
S Fert-Ferrer, A Guichet, J Tantau, et al.
Human Mutation
|
July 5, 2001
Twelve novel mutations in the tissue-nonspecific alkaline phosphatase gene (ALPL) in patients with various forms of hypophosphatasia
A Taillandier, A S Lia-Baldini, M Mouchard, et al.
Clinical Genetics
|
September 26, 2015
Fetal phenotypes in otopalatodigital spectrum disorders
S Naudion, S Moutton, I Coupry, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 49) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 49 results.
American Journal of Medical Genetics. Part A
|
September 27, 2014
Inverted duplication with deletion: first interstitial case suggesting a novel undescribed mechanism of formation
J Milosevic, L El Khattabi, A Roubergue, et al.
Prenatal Diagnosis
|
March 12, 1999
Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature
L Faivre, N Morichon-Delvallez, G Viot, et al.
Journal of Medical Genetics
|
October 4, 2002
Homozygosity mapping of a Dyggve-Melchior-Clausen syndrome gene to chromosome 18q21.1
C Thauvin-Robinet, V El Ghouzzi, W Chemaitilly, et al.
Gynecologie, Obstetrique, Fertilite & Senologie
|
February 15, 2020
[Adverse obstetric and perinatal outcome with in vitro fertilization technology: A French nationwide population-based study]
F Pessione, J De Mouzon, A Deveaux, et al.
Clinical Genetics
|
January 11, 2016
Complex mode of inheritance in holoprosencephaly revealed by whole exome sequencing
C Mouden, C Dubourg, W Carré, et al.
The Journal of Pediatrics
|
July 11, 2001
Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome
H De Leersnyder, M C De Blois, B Claustrat, et al.
Prenatal Diagnosis
|
June 22, 2000
Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann features
S Fert-Ferrer, A Guichet, J Tantau, et al.
Human Mutation
|
July 5, 2001
Twelve novel mutations in the tissue-nonspecific alkaline phosphatase gene (ALPL) in patients with various forms of hypophosphatasia
A Taillandier, A S Lia-Baldini, M Mouchard, et al.
Clinical Genetics
|
September 26, 2015
Fetal phenotypes in otopalatodigital spectrum disorders
S Naudion, S Moutton, I Coupry, et al.
Page
of 5