Herens C - Search Results

1

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: herens c. Genet Couns. 1992;3(3):155-9. Genet Couns. 1992. PMID: 1388935

2

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: herens c. Genet Couns. 1991;2(2):123-7. Genet Couns. 1991. PMID: 1781957

3

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

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

4

Branchial arch anomalies in trisomy 18.

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

5

Mosaicism of 46,XX/47,XX,+9/47,XX,+?mar in the same amniotic fluid with apparent loss of one cell line after delivery.

Herens C, Pierquin G, Verloes A, Schaaps JP, Frederic J. Herens C, et al. Prenat Diagn. 1989 May;9(5):373-5. doi: 10.1002/pd.1970090513. Prenat Diagn. 1989. PMID: 2726702

6

Roberts-SC phocomelia syndrome with exencephaly.

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

7

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

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

8

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. Among authors: herens c. 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

9

Monosomy 11q: report of two familial cases and review of the literature.

Hustinx R, Verloes A, Grattagliano B, Herens C, Jamar M, Soyeur D, Schaaps JP, Koulischer L. Hustinx R, et al. Among authors: herens c. Am J Med Genet. 1993 Sep 1;47(3):312-7. doi: 10.1002/ajmg.1320470303. Am J Med Genet. 1993. PMID: 8135272 Review.

10

Private multiple congenital anomaly syndromes may result from unbalanced subtle translocations: t(2q;4p) explains the Lambotte syndrome.

Herens C, Jamar M, Alvarez-Gonzalez ML, Lesenfants S, Lombet J, Bonnivert J, Koulischer L, Verloes A. Herens C, et al. Am J Med Genet. 1997 Dec 12;73(2):127-31. doi: 10.1002/(sici)1096-8628(19971212)73:2<127::aid-ajmg5>3.0.co;2-r. Am J Med Genet. 1997. PMID: 9409861

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