Publications - Revision history

Serveradmin at 15:27, 24 June 2020

2020-06-24T15:27:20Z

Serveradmin at 15:27, 24 June 2020

2020-06-24T15:27:05Z

Serveradmin at 15:26, 24 June 2020

2020-06-24T15:26:14Z

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Serveradmin: Created page with "* Musarella MA, Anson Cartwright L, Leal SM, Gilbert LD, Worton RG, Fishman GA, Ott J (1990) Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pig..."

2020-06-24T15:23:40Z

Created page with "* Musarella MA, Anson Cartwright L, Leal SM, Gilbert LD, Worton RG, Fishman GA, Ott J (1990) Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pig..."

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 '''Lasted updated: May, 2020'''
-* Hussain S, Nawaz S, Khan H, Acharya A, Schrauwen I, Ahmad W, Leal SM (2020) A splice site variant in ''TCTN3'' underlies orofaciodigital syndrome IV. (submittd)
+* Hussain S, Nawaz S, Khan H, Acharya A, Schrauwen I, Ahmad W, Leal SM (2020) A splice site variant in ''TCTN3'' underlies orofaciodigital syndrome IV. (submitted)
 * Schrauwen I, Liaqat K, Bharadwaj T, Nasir A, Acharya A, Ahmad W, Leal SM (2020) An Autosomal Dominantly inherited variant in ''GREB1L'' causes profound sensorineural hearing impairment (submitted)
 * Hirsch S, Elling C, Bootpetch Roberts TC, Scholes MA, Hafrén L. Streubel SO, Pine HS, Wine TM, Szeremeta W, Prager JD, Elisabet Einarsdottir E, Yousaf A, Baschal EE, Sakina Rehman S, University of Washington Center for Mendelian Genomics, Bamshad MJ, Nickerson DA, Riazuddin S, Leal SM, Ahmed ZM, Yoon PJ, Kere J, Chan KH, MattilaPS, Norman R. Friedman NR, Chonmaitree T, Frank DN, Ryan AF, Santos-Cortez RLP (2020) The role of ''CDHR3 ''in susceptibility to otitis media (submitted)

← Older revision		Revision as of 15:27, 24 June 2020
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		+	'''Lasted updated: May, 2020'''
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	* Hussain S, Nawaz S, Khan H, Acharya A, Schrauwen I, Ahmad W, Leal SM (2020) A splice site variant in ''TCTN3'' underlies orofaciodigital syndrome IV. (submittd)		* Hussain S, Nawaz S, Khan H, Acharya A, Schrauwen I, Ahmad W, Leal SM (2020) A splice site variant in ''TCTN3'' underlies orofaciodigital syndrome IV. (submittd)
	* Schrauwen I, Liaqat K, Bharadwaj T, Nasir A, Acharya A, Ahmad W, Leal SM (2020) An Autosomal Dominantly inherited variant in ''GREB1L'' causes profound sensorineural hearing impairment (submitted)		* Schrauwen I, Liaqat K, Bharadwaj T, Nasir A, Acharya A, Ahmad W, Leal SM (2020) An Autosomal Dominantly inherited variant in ''GREB1L'' causes profound sensorineural hearing impairment (submitted)