Your search returned 187 results.

Results
	1.	[POSSUM. Computer assisted diagnosis in medical genetic]. [electronic resource] by Le Merrer, M Producer: 19920611 In: La Revue du praticien vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	2.	Acrodysgenital dwarfism or Smith-Lemli-Opitz type II syndrome. [electronic resource] by Le Merrer, M Producer: 19920305 In: Clinical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	[Congenital malformations--multiple abnormalities syndromes]. [electronic resource] by le Merrer, M Producer: 19900801 In: Soins. Gynecologie, obstetrique, puericulture, pediatrie no. 106 Availability: No items available. Save to lists Add to cart (remove)
	4.	Lumping of CFC and Baraitser-Patton Noonan-like syndromes. [electronic resource] by Verloes, A Le Merrer, M Producer: 19920818 In: American journal of medical genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	[Battered or brittle child?]. [electronic resource] by Maroteaux, P Le Merrer, M Producer: 20031104 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Bilateral Poland anomaly versus thoracic dysplasia. [electronic resource] by Maroteaux, P Le Merrer, M Producer: 19990310 In: American journal of medical genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Metaphyseal anadysplasia type II: a new regressive metaphyseal dysplasia. [electronic resource] by Le Merrer, M Maroteaux, P Producer: 19990105 In: Pediatric radiology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Cartilage hair hypoplasia in infancy: a misleading chondrodysplasia. [electronic resource] by Le Merrer, M Maroteaux, P Producer: 19920114 In: European journal of pediatrics vol. 150 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	[Unusual familial malformation of the hand]. [electronic resource] by Le Merrer, M Frézal, J Producer: 19830826 In: Journal de genetique humaine vol. 30 Suppl 5 Availability: No items available. Save to lists Add to cart (remove)
	10.	Clinical approach still has an important role in constitutional bone diseases. [electronic resource] by Maroteaux, P Le Merrer, M Producer: 19970605 In: Journal of pediatric orthopedics. Part B vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Dwarfism with gloomy face: a new syndrome with features of 3-M syndrome. [electronic resource] by Le Merrer, M Brauner, R Maroteaux, P Producer: 19910723 In: Journal of medical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	[Familial acrocephalosyndactylia]. [electronic resource] by Le Merrer, M Maroteaux, P Frézal, J Producer: 19840214 In: Annales de pediatrie vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	13.	Spondyloepimetaphyseal dysplasia with multiple dislocations, leptodactylic type: report of a new patient and review of the literature. [electronic resource] by Mégarbané, A Ghanem, I Le Merrer, M Producer: 20040422 In: American journal of medical genetics. Part A vol. 122A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Genochondromatosis. [electronic resource] by Le Merrer, M Fressinger, P Maroteaux, P Producer: 19911021 In: Journal of medical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Pachydysostosis of the fibula. [electronic resource] by Maroteaux, P Freisinger, P Le Merrer, M Producer: 19911023 In: The Journal of bone and joint surgery. British volume vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Scalp defect, absence of nipples, ear anomalies, renal hypoplasia: another case of Finlay-Marks syndrome. [electronic resource] by Plessis, G Le Treust, M Le Merrer, M Producer: 19980121 In: Clinical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Scalp defect, nipples absence and ears abnormalities: an other case of Finlay syndrome. [electronic resource] by Le Merrer, M Renier, D Briard, M L Producer: 19920421 In: Genetic counseling (Geneva, Switzerland) vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	18.	[Ectodermal dysplasia and familial ectrodactyly]. [electronic resource] by Predine-Hug, F Le Merrer, M Frézal, J Producer: 19840530 In: Archives francaises de pediatrie vol. 41 Availability: No items available. Save to lists Add to cart (remove)
	19.	Ptosis, down-slanting palpebral fissures, hypertelorism, seizures and mental retardation: a possible new MCA/MR syndrome. [electronic resource] by Mégarbané, A Le Merrer, M el Kallab, K Producer: 19970922 In: Clinical dysmorphology vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	BBBG syndrome or Opitz syndrome: new family. [electronic resource] by Verloes, A Le Merrer, M Briard, M L Producer: 19900112 In: American journal of medical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

1
2
3
4
5
6
7
8
9
10
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 187 results.