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Page 1
Prenatal diagnosis by FISH of a 22q11 deletion in two families.
J Med Genet. 1998 Feb;35(2):165-8. doi: 10.1136/jmg.35.2.165.
J Med Genet. 1998.
PMID: 9507401
Free PMC article.
Karyotypes of 1142 couples with recurrent abortion.
Portnoï MF, Joye N, van den Akker J, Morlier G, Taillemite JL.
Portnoï MF, et al. Among authors: morlier g.
Obstet Gynecol. 1988 Jul;72(1):31-4.
Obstet Gynecol. 1988.
PMID: 3242501
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Skin pigmentary anomalies and mosaicism for an acentric marker chromosome originating from 3q.
Portnoï MF, Boutchneï S, Bouscarat F, Morlier G, Nizard S, Dersarkissian H, Crickx B, Nouchy M, Taillemite JL, Belaich S.
Portnoï MF, et al. Among authors: morlier g.
J Med Genet. 1999 Mar;36(3):246-50.
J Med Genet. 1999.
PMID: 10204855
Free PMC article.
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[Turner syndrome: mosaic and isochromosome q in a young African woman].
Mensah-Ado I, Lauhbouet MD, Lokrou A, Ehouman A, Morlier G.
Mensah-Ado I, et al. Among authors: morlier g.
Med Trop (Mars). 1994;54(4):349-51.
Med Trop (Mars). 1994.
PMID: 7746129
French.
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[1st case of eosinophilic meningitis in Ivory Coat with the presence of a Parastrongylus sp. in the cerebrospinal fluid].
Nozais JP, Moreau J, Morlier G, Kouame J, Doucet J.
Nozais JP, et al. Among authors: morlier g.
Bull Soc Pathol Exot Filiales. 1980 Mar-Apr;73(2):179-82.
Bull Soc Pathol Exot Filiales. 1980.
PMID: 6257411
French.
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