Koulischer L - 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: koulischer l. Genet Couns. 1992;3(3):155-9. Genet Couns. 1992. PMID: 1388935

2

Male pseudohermaphroditism with persistent müllerian structures, mental retardation and Borjeson-Forssman-Lehmann-like features: a new syndrome?

Verloes A, Gillerot Y, Delfortrie J, Zeevaert-Arnold MT, Collard R, Koulischer L, Fryns JP. Verloes A, et al. Among authors: koulischer l. Genet Couns. 1990;1(3-4):219-25. Genet Couns. 1990. PMID: 2098045

3

Microcephaly, macrotia, unusual mimics and mental retardation syndrome: new syndrome or variant of De Lange type 2 syndrome.

Verloes A, Lesenfants S, Philippet B, Iyawa A, Laloux F, Koulischer L. Verloes A, et al. Among authors: koulischer l. Genet Couns. 1996;7(4):277-82. Genet Couns. 1996. PMID: 8985731

4

New oral-acral syndrome with partial agenesis of the maxillary bones.

Verloes A, Koulischer L. Verloes A, et al. Among authors: koulischer l. Am J Med Genet. 1992 Nov 15;44(5):605-7. doi: 10.1002/ajmg.1320440514. Am J Med Genet. 1992. PMID: 1481817

5

Variability versus heterogeneity in syndromal hypothalamic hamartoblastoma and related disorders: review and delineation of the cerebro-acro-visceral early lethality (CAVE) multiplex syndrome.

Verloes A, Gillerot Y, Langhendries JP, Fryns JP, Koulischer L. Verloes A, et al. Among authors: koulischer l. Am J Med Genet. 1992 Jul 1;43(4):669-77. doi: 10.1002/ajmg.1320430404. Am J Med Genet. 1992. PMID: 1621756 Review.

6

Acromelic frontonasal "dysplasia": further delineation of a subtype with brain malformation and polydactyly (Toriello syndrome).

Verloes A, Gillerot Y, Walczak E, Van Maldergem L, Koulischer L. Verloes A, et al. Among authors: koulischer l. Am J Med Genet. 1992 Jan 15;42(2):180-3. doi: 10.1002/ajmg.1320420209. Am J Med Genet. 1992. PMID: 1733166 Review.

7

Branchial arch anomalies in trisomy 18.

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

8

Campomelic syndrome: manifestations in a 20 week fetus and case history of a 5 year old child.

Gillerot Y, Vanheck CA, Foulon M, Podevain A, Koulischer L. Gillerot Y, et al. Among authors: koulischer l. Am J Med Genet. 1989 Dec;34(4):589-92. doi: 10.1002/ajmg.1320340428. Am J Med Genet. 1989. PMID: 2624275

9

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: koulischer l. 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

10

Diabetes mellitus, mental retardation, lipodystrophy and dysmorphic traits.

Verloes A, Ernould C, Dubru JM, Malchair R, Koulischer L. Verloes A, et al. Among authors: koulischer l. Clin Dysmorphol. 1994 Apr;3(2):160-3. Clin Dysmorphol. 1994. PMID: 8055137

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

123 results

Search Page

Filters