Your search returned 1610 results.

Results
	1121.	Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome. [electronic resource] by Kohlhase, J Wischermann, A Reichenbach, H Froster, U Engel, W Producer: 19980129 In: Nature genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1122.	-A difficult intubation of an infant with McKusick-Kaufman syndrome. Failure of the laryngeal mask-fibroscope sequence-. [electronic resource] by el Hammar, F Dubreuil, M Benoît, I Meymat, Y Producer: 19981022 In: Annales francaises d'anesthesie et de reanimation vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1123.	Familial acromelic frontonasal dysostosis: autosomal dominant inheritance with reduced penetrance. [electronic resource] by Hing, Anne V Syed, Nadia Cunningham, Michael L Producer: 20050218 In: American journal of medical genetics. Part A vol. 128A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1124.	Prenatal diagnosis of a case probably with Oral-Facial-Digital Syndrome--Gabrielli type. [electronic resource] by Güven, M A Ceylaner, G Ceylaner, S Uzel, M Coskun, A Producer: 20090928 In: Genetic counseling (Geneva, Switzerland) vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	1125.	Idiopathic hemihypertrophy. [electronic resource] by Mohanna, Mabrook A Sallam, Abdul Khalig Producer: 20150413 In: Saudi medical journal vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	1126.	[SURGICAL TREATMENT OF CONGENITAL TYPE V THUMB SYNDACTYLY]. [electronic resource] by Tang, Haipeng Sun, Guangfeng Qi, Jianping Nie, Kaiyu Jin, Wenhu Li, Shujun Wei, Zairong Wang, Dali Producer: 20181108 In: Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1127.	Oral-facial-digital syndrome II. Transitional type between Mohr and Majewski syndrome: report of a new case with congenital stenosis of the trachea. [electronic resource] by Steichen-Gersdorf, E Gassner, I Covi, B Fischer, H Producer: 19950103 In: Clinical dysmorphology vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	1128.	Early sonographic aspects of kidney morphology in Bardet-Biedl syndrome. [electronic resource] by Dippell, J Varlam, D E Producer: 19990108 In: Pediatric nephrology (Berlin, Germany) vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1129.	[Prenatal diagnosis. II. Importance of ultrasonographic markers in prenatal diagnosis of chromosome abnormalities]. [electronic resource] by Prieto-Carrasquero, M Molero, A Carrasquero, N Del Villar, A González-Ferrer, S Rojas, A Brito, J Mena, R González, L Pérez, F Alvarez, F Quintero, M Fulcado, W Producer: 19990222 In: Investigacion clinica vol. 39 Availability: No items available. Save to lists Add to cart (remove)
	1130.	Meckel syndrome: genetics, perinatal findings, and differential diagnosis. [electronic resource] by Chen, Chih-Ping Producer: 20070612 In: Taiwanese journal of obstetrics & gynecology vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1131.	Identification of CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzle. [electronic resource] by Tallila, Jonna Jakkula, Eveliina Peltonen, Leena Salonen, Riitta Kestilä, Marjo Producer: 20080627 In: American journal of human genetics vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1132.	The clinical atlas of Greig cephalopolysyndactyly syndrome. [electronic resource] by Balk, Katherine Biesecker, Leslie G Producer: 20080507 In: American journal of medical genetics. Part A vol. 146A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1133.	Subcutaneous polypoid lipoma of the first intermetatarsal space mimicking rudimentary polydactyly. [electronic resource] by Decker, Joshua Husain, Zeeshan S Kissel, Charles G David, Doina Wehrli, Benjamin Producer: 20101019 In: The Journal of foot and ankle surgery : official publication of the American College of Foot and Ankle Surgeons vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1134.	Preaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis-regulatory element ZRS. [electronic resource] by Farooq, Muhammad Troelsen, Jesper T Boyd, Mette Eiberg, Hans Hansen, Lars Hussain, Muhammad Sajid Rehman, Shoaib ur Azhar, Aysha Ali, Amjad Bakhtiar, Syeda Marriam Tommerup, Niels Baig, Shahid Mahmood Kjaer, Klaus W Producer: 20100908 In: European journal of human genetics : EJHG vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1135.	Hydrometrocolpos Presenting as a Huge Abdominal Swelling and Obstructive Uropathy in a 4 Day Old Newborn: A Diagnostic Challenge. [electronic resource] by Tilahun, Birkneh Woldegebriel, Fitsum Wolde, Zenebe Tadele, Henok Producer: 20161213 In: Ethiopian journal of health sciences vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1136.	Familial short rib syndrome, type Beemer, with pyloric stenosis and short intestine, one case diagnosed prenatally. [electronic resource] by Balci, S Erçal, M D Onol, B Cağlar, M Doğan, A Doğruel, N Producer: 19910822 In: Clinical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1137.	Interstitial deletion of the long arm of chromosome 4 [del(4)(q21.22q23)] and a liver tumor. [electronic resource] by Suwa, K Momoi, M Y Yamagata, T Mori, Y Producer: 19980923 In: American journal of medical genetics vol. 78 Availability: No items available. Save to lists Add to cart (remove)
	1138.	Genitourinary malformations as a feature of the Pallister-Hall syndrome. [electronic resource] by McCann, Emma Fryer, Alan E Craigie, Ross Baillie, Colin Ba'ath, Muhammed E Selby, Andrew Biesecker, Leslie G Producer: 20090107 In: Clinical dysmorphology vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1139.	Simplicity and treatment of the typical cleft hand. [electronic resource] by Upton, J Producer: 20040908 In: Handchirurgie, Mikrochirurgie, plastische Chirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft fur Handchirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft fur Mikrochirurgie der Peripheren Nerven und Gefasse : Organ der V vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1140.	[Active and passive maternal smoking during pregnancy and risk of having a child with polydactyly: a case-control study]. [electronic resource] by Shi, J Tian, Y Lei, Y Kang, H Producer: 20190228 In: Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

First
Previous
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 1610 results.