Verloes A - Search Results

1

Prenatal diagnosis of cystic hygroma and chorioangioma in the Wolf-Hirschhorn syndrome.

Verloes A, Schaaps JP, Herens C, Soyeur D, Hustin J, Dodinval P. Verloes A, et al. Prenat Diagn. 1991 Feb;11(2):129-32. doi: 10.1002/pd.1970110209. Prenat Diagn. 1991. PMID: 2062819

2

Combined 10pter-->p11 and 18pter-->q11 trisomy in a 7-year-old child.

Lapière JC, Verloes A, Herens C, Delfortrie J, Van Maldergem L, Gillerot Y, Koulischer L. Lapière JC, et al. Among authors: verloes a. Genet Couns. 1992;3(3):155-9. Genet Couns. 1992. PMID: 1388935

3

Glaucoma-lens ectopia-microspherophakia-stiffness-shortness (GEMSS) syndrome: a dominant disease with manifestations of Weill-Marchesani syndromes.

Verloes A, Hermia JP, Galand A, Koulischer L, Dodinval P. Verloes A, et al. Am J Med Genet. 1992 Sep 1;44(1):48-51. doi: 10.1002/ajmg.1320440112. Am J Med Genet. 1992. PMID: 1519650

4

[Prenatal screening for trisomy 21 in maternal blood. Focus].

Koulischer L, Schoos R, Verloes A, Herens C. Koulischer L, et al. Among authors: verloes a. Rev Med Liege. 1991 Dec;46(12):625-32. Rev Med Liege. 1991. PMID: 1722586 French. No abstract available.

5

A hydropic fetus with translucent ribs, arthrogryposis multiplex congenita and congenital myopathy: etiological heterogeneity of A.M.C., Toriello-Bauserman type?

Verloes A, Dodinval P, Retz MC, Schaaps JP, Koulischer L. Verloes A, et al. Genet Couns. 1991;2(1):63-6. Genet Couns. 1991. PMID: 1741979 No abstract available.

6

Ring chromosome 9 in a newborn male presenting with facial dysmorphia, hypospadias and skeletal abnormalities.

Van Maldergem L, Avni F, Mossay B, Herens C, Verloes A, Gillerot Y. Van Maldergem L, et al. Among authors: verloes a. Genet Couns. 1991;2(2):123-7. Genet Couns. 1991. PMID: 1781957

7

Branchial arch anomalies in trisomy 18.

Verloes A, Seret N, Bernier V, Gonzales M, Herens C, Koulischer L. Verloes A, et al. Ann Genet. 1991;34(1):22-4. Ann Genet. 1991. PMID: 1952786

8

Trisomy 20q. A new case and further phenotypic delineation.

Herens C, Verloes A, Laloux F, Van Maldergem L. Herens C, et al. Among authors: verloes a. Clin Genet. 1990 May;37(5):363-6. doi: 10.1111/j.1399-0004.1990.tb03520.x. Clin Genet. 1990. PMID: 2191794 Review.

9

Lambotte syndrome: microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethality--a new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs.

Verloes A, Dodinval P, Beco L, Bonnivert J, Lambotte C. Verloes A, et al. Am J Med Genet. 1990 Sep;37(1):119-23. doi: 10.1002/ajmg.1320370128. Am J Med Genet. 1990. PMID: 2240028

10

Poikiloderma, alopecia, retrognathism and cleft palate: the PARC syndrome. Is this an undescribed dominantly inherited syndrome?

Verloes A, Soyeur-Broux M, Arrese-Estrada J, Piérard-Franchimont C, Dodinval P, Piérard GE. Verloes A, et al. Dermatologica. 1990;181(2):142-4. doi: 10.1159/000247904. Dermatologica. 1990. PMID: 2242783

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