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Genotype determination at the survival motor neuron locus in a normal population and SMA carriers using competitive PCR and primer extension. [electronic resource] by
- Gérard, B
- Ginet, N
- Matthijs, G
- Evrard, P
- Baumann, C
- Da Silva, F
- Gérard-Blanluet, M
- Mayer, M
- Grandchamp, B
- Elion, J
Producer: 20001030
In:
Human mutation vol. 16
Availability: No items available.
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Prenatal detection of Pierre Robin sequence with deletion Xp and additional trisomy 14q by telomere screening. [electronic resource] by
- Gerard-Blanluet, M
- Pipiras, E
- Levaillant, J M
- Joye, N
- Koubi, V
- Kanafani, S
- Vergnaud, A
- Verloes, A
- Gonzales, M
- Jeny, R
- Benzacken, B
Producer: 20080211
In:
Prenatal diagnosis vol. 27
Availability: No items available.
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7.
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Prenatal forehead edema in 4p- deletion: the 'Greek warrior helmet' profile revisited. [electronic resource] by
- Levaillant, J M
- Touboul, C
- Sinico, M
- Vergnaud, A
- Serero, S
- Druart, L
- Blondeau, J R
- Abd Alsamad, I
- Haddad, B
- Gérard-Blanluet, M
Producer: 20070129
In:
Prenatal diagnosis vol. 25
Availability: No items available.
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8.
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Binder phenotype in mothers affected with autoimmune disorders. [electronic resource] by
- Colin, E
- Touraine, R
- Levaillant, J M
- Pasquier, L
- Boussion, F
- Ferry, M
- Guichet, A
- Barth, M
- Mercier, A
- Gérard-Blanluet, M
- Odent, S
- Bonneau, D
Producer: 20130110
In:
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians vol. 25
Availability: No items available.
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De novo subtelomeric deletion additional to an inherited apparently balanced reciprocal translocation. [electronic resource] by
- Delahaye, A
- Pipiras, E
- Kanafani, S
- Touboul, C
- Vergnaud, A
- Encha-Razavi, F
- Sinico, M
- Benkhalifa, M
- Kasakyan, S
- Serero, S
- Wolf, J P
- Gérard-Blanluet, M
- Benzacken, B
Producer: 20070703
In:
Fetal diagnosis and therapy vol. 22
Availability: No items available.
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10.
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2q23.1 microdeletion identified by array comparative genomic hybridisation: an emerging phenotype with Angelman-like features? [electronic resource] by
- Jaillard, S
- Dubourg, C
- Gérard-Blanluet, M
- Delahaye, A
- Pasquier, L
- Dupont, C
- Henry, C
- Tabet, A-C
- Lucas, J
- Aboura, A
- David, V
- Benzacken, B
- Odent, S
- Pipiras, E
Producer: 20100311
In:
Journal of medical genetics vol. 46
Availability: No items available.
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11.
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Binder phenotype: clinical and etiological heterogeneity of the so-called Binder maxillonasal dysplasia in prenatally diagnosed cases, and review of the literature. [electronic resource] by
- Levaillant, J M
- Moeglin, D
- Zouiten, K
- Bucourt, M
- Burglen, L
- Soupre, V
- Baumann, C
- Jaquemont, M L
- Touraine, R
- Picard, A
- Vuillard, E
- Belarbi, N
- Oury, J F
- Verloes, A
- Vazquez, M P
- Labrune, P
- Delezoide, A L
- Gérard-Blanluet, M
Producer: 20090505
In:
Prenatal diagnosis vol. 29
Availability: No items available.
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