Lacombe D - Search Results

1

Ondine-Hirschsprung syndrome (Haddad syndrome). Further delineation in two cases and review of the literature.

Verloes A, Elmer C, Lacombe D, Heinrichs C, Rebuffat E, Demarquez JL, Moncla A, Adam E. Verloes A, et al. Among authors: lacombe d. Eur J Pediatr. 1993 Jan;152(1):75-7. doi: 10.1007/BF02072522. Eur J Pediatr. 1993. PMID: 8444212 Review.

2

[Loperamide and acute diarrhea in infants].

Lamireau T, Fayon M, Rigot A, Lacombe D, Hehunstre JP, Sarlangue J, Demarquez JL. Lamireau T, et al. Among authors: lacombe d. Arch Fr Pediatr. 1991 Nov;48(9):665. Arch Fr Pediatr. 1991. PMID: 1763939 French. No abstract available.

3

Neonatal Noonan syndrome with a molluscoid cutaneous excess over the scalp.

Lacombe D, Taieb A, Masson P, Fayon M, Demarquez JL. Lacombe D, et al. Genet Couns. 1991;2(4):249-53. Genet Couns. 1991. PMID: 1799426

4

Floating-Harbor syndrome: description of a further patient, review of the literature, and suggestion of autosomal dominant inheritance.

Lacombe D, Patton MA, Elleau C, Battin J. Lacombe D, et al. Eur J Pediatr. 1995 Aug;154(8):658-61. doi: 10.1007/BF02079072. Eur J Pediatr. 1995. PMID: 7588969 Review.

5

Lujan-Fryns syndrome (X-linked mental retardation with marfanoid habitus): report of three cases and review.

Lacombe D, Bonneau D, Verloes A, Couet D, Koulischer L, Battin J. Lacombe D, et al. Genet Couns. 1993;4(3):193-8. Genet Couns. 1993. PMID: 8267926

6

[Unusual form of Noonan syndrome: neonatal multi-organ involvement with chylothorax and nevoid Cutis verticis gyrata].

Masson P, Fayon M, Lamireau T, Llanas B, Lacombe D, Taïeb A, Demarquez JL. Masson P, et al. Among authors: lacombe d. Pediatrie. 1993;48(1):59-62. Pediatrie. 1993. PMID: 8392694 French.

7

Phenotypic variability in van der Woude syndrome.

Lacombe D, Pedespan JM, Fontan D, Chateil JF, Verloes A. Lacombe D, et al. Genet Couns. 1995;6(3):221-6. Genet Couns. 1995. PMID: 8588850

8

[Smith-Magenis syndrome].

Lacombe D, Moncla A, Malzac P, Mattei MG, Battin J. Lacombe D, et al. Arch Pediatr. 1997 May;4(5):438-42. doi: 10.1016/s0929-693x(97)86671-7. Arch Pediatr. 1997. PMID: 9230994 French.

9

Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism.

Karadima G, Bugge M, Nicolaidis P, Vassilopoulos D, Avramopoulos D, Grigoriadou M, Albrecht B, Passarge E, Annerén G, Blennow E, Clausen N, Galla-Voumvouraki A, Tsezou A, Kitsiou-Tzeli S, Hahnemann JM, Hertz JM, Houge G, Kuklík M, Macek M, Lacombe D, Miller K, Moncla A, López Pajares I, Patsalis PC, Petersen MB, et al. Karadima G, et al. Among authors: lacombe d. Eur J Hum Genet. 1998 Sep-Oct;6(5):432-8. doi: 10.1038/sj.ejhg.5200212. Eur J Hum Genet. 1998. PMID: 9801867

10

Hydrometrocolpos and polydactyly: a common neonatal presentation of Bardet-Biedl and McKusick-Kaufman syndromes.

David A, Bitoun P, Lacombe D, Lambert JC, Nivelon A, Vigneron J, Verloes A. David A, et al. Among authors: lacombe d. J Med Genet. 1999 Aug;36(8):599-603. J Med Genet. 1999. PMID: 10465109 Free PMC article.

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

676 results

Search Page

Filters