Manouvrier-Hanu S - Search Results

1

Crane-Heise syndrome: two further case reports.

Petit F, Devisme L, Toutain A, Houfflin-Debarge V, Dieux-Coeslier A, Manouvrier-Hanu S, Andrieux J, Holder-Espinasse M. Petit F, et al. Eur J Med Genet. 2011 Mar-Apr;54(2):169-72. doi: 10.1016/j.ejmg.2010.11.004. Epub 2010 Nov 20. Eur J Med Genet. 2011. PMID: 21094705

2

Severe combined immunodeficiency syndrome associated with autosomal recessive familial multiple gastrointestinal atresias: study of a family.

Moreno LA, Gottrand F, Turck D, Manouvrier-Hanu S, Mazingue F, Morisot C, Le Deist F, Ricour C, Nihoul-Feketé C, Debeugny P, et al. Moreno LA, et al. Am J Med Genet. 1990 Sep;37(1):143-6. doi: 10.1002/ajmg.1320370133. Am J Med Genet. 1990. PMID: 2240032

3

Prenatal diagnosis of metatropic dwarfism.

Manouvrier-Hanu S, Devisme L, Zelasko MC, Bourgeot P, Vincent-Delorme C, Valat-Rigot AS, Puech F, Farriaux JP. Manouvrier-Hanu S, et al. Prenat Diagn. 1995 Aug;15(8):753-6. doi: 10.1002/pd.1970150811. Prenat Diagn. 1995. PMID: 7479594

4

Fryns syndrome and erupted teeth in a 24-weeks-old fetus.

Manouvrier-Hanu S, Devisme L, Vaast P, Boute-Benejean O, Farriaux JP. Manouvrier-Hanu S, et al. Genet Couns. 1996;7(2):131-4. Genet Couns. 1996. PMID: 8831132

5

Pulmonary hypertension of the newborn and urogenital anomalies in two male siblings: a new family with misalignment of pulmonary vessels.

Manouvrier-Hanu S, Devisme L, Farre I, Hue V, Storme L, Kacet N, Boute-Benejean O, Farriaux JP. Manouvrier-Hanu S, et al. Genet Couns. 1996;7(4):249-55. Genet Couns. 1996. PMID: 8985728

6

Genetics of limb anomalies in humans.

Manouvrier-Hanu S, Holder-Espinasse M, Lyonnet S. Manouvrier-Hanu S, et al. Trends Genet. 1999 Oct;15(10):409-17. doi: 10.1016/s0168-9525(99)01823-5. Trends Genet. 1999. PMID: 10498937 Review.

7

Unreported RSK2 missense mutation in two male sibs with an unusually mild form of Coffin-Lowry syndrome.

Manouvrier-Hanu S, Amiel J, Jacquot S, Merienne K, Moerman A, Coëslier A, Labarriere F, Vallée L, Croquette MF, Hanauer A. Manouvrier-Hanu S, et al. J Med Genet. 1999 Oct;36(10):775-8. doi: 10.1136/jmg.36.10.775. J Med Genet. 1999. PMID: 10528858 Free PMC article.

8

The Richieri-Costa and Pereira form of acrofacial dysostosis: first case in a non-Brazilian infant.

Walter-Nicolet E, Coëslier A, Joriot S, Kacet N, Moerman A, Manouvrier-Hanu S. Walter-Nicolet E, et al. Am J Med Genet. 1999 Dec 22;87(5):430-3. doi: 10.1002/(sici)1096-8628(19991222)87:5<430::aid-ajmg11>3.0.co;2-9. Am J Med Genet. 1999. PMID: 10594883 Review.

9

Sex reversal and diaphragmatic hernia in phenotypicaly female sibs with normal XY chromosomes.

Manouvrier-Hanu S, Besson R, Cousin L, Jeanpierre C, Kacet N, Cartigny M, Devisme L, Storme L, De Martinville B, Lequien P. Manouvrier-Hanu S, et al. J Med Genet. 2000 Apr;37(4):315-8. doi: 10.1136/jmg.37.4.315. J Med Genet. 2000. PMID: 10819644 Free PMC article. Review. No abstract available.

10

[Value of fetopathological examination in medical abortions: comparison of prenatal diagnosis and autopsy results of 300 fetuses].

Laussel-Riera A, Devisme L, Manouvrier-Hanu S, Puech F, Robert Y, Gosselin B. Laussel-Riera A, et al. Ann Pathol. 2000 Dec;20(6):549-57. Ann Pathol. 2000. PMID: 11148350 French.

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