Verloes A - Search Results

1

Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.

Riegel M, Baumer A, Jamar M, Delbecque K, Herens C, Verloes A, Schinzel A. Riegel M, et al. Among authors: verloes a. Hum Genet. 2001 Sep;109(3):286-94. doi: 10.1007/s004390100585. Hum Genet. 2001. PMID: 11702209

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

[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.

4

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

5

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

6

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

7

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.

8

Roberts-SC phocomelia syndrome with exencephaly.

Verloes A, Herens C, Van Maldergem L, Retz MC, Dodinval P. Verloes A, et al. Ann Genet. 1989;32(3):169-70. Ann Genet. 1989. PMID: 2817778

9

Chromosome 22 mosaic monosomy (46,XY/45,XY,-22).

Verloes A, Herens C, Lambotte C, Frederic J. Verloes A, et al. Ann Genet. 1987;30(3):178-9. Ann Genet. 1987. PMID: 3499857

10

A prenatal trisomy 21 screening program using alpha-fetoprotein, human chorionic gonadotropin, and free estriol assays on maternal dried blood.

Verloes A, Schoos R, Herens C, Vintens A, Koulischer L. Verloes A, et al. Am J Obstet Gynecol. 1995 Jan;172(1 Pt 1):167-74. doi: 10.1016/0002-9378(95)90108-6. Am J Obstet Gynecol. 1995. PMID: 7531397

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